Fungicidal compositions

ABSTRACT

The present invention provides a composition comprising a combination of components A) and B), wherein component A) is a compound of formula (I) 
     
       
         
         
             
             
         
       
         
         
           
             and the component (B) is a further fungicide, insecticide or herbicide.

RELATED APPLICATION INFORMATION

This application is a divisional of U.S. patent application Ser. No. 14/362,709 filed on 4 Jun. 2014, which is a 371 of International Application No. PCT/CN2012/073665, filed 9 Apr. 2012, which claims priority to International Application No. PCT/CN2011/084016, filed 14 Dec. 2011, the contents of which are incorporated herein by reference.

The present invention relates to novel fungicidal compositions which comprise fungicidally active pyridylamidine compounds for the treatment of phytopathogenic diseases of useful plants, especially phytopathogenic fungi, and to a method of controlling phytopathogenic diseases on useful plants.

Certain phenylamidine derivatives are described in WO2008/101682 as microbicidally active ingredients in pesticides.

The present invention provides a composition comprising a combination of components A) and B), wherein component A) is a compound of formula (I)

-   -   wherein     -   R₁ and R₂ are each independently selected from hydrogen, C₁-C₄         alkyl, C₃-C₄ alkenyl, C₃-C₄ alkynyl, (R₁₀)carbonyl and         (R₁₀)oxycarbonyl;     -   or R₁ and R₂ together with the nitrogen atom to which they are         attached form a 5- or 6 membered cyclic group which may be         saturated or unsaturated and may contain a further heteroatom         selected from S or O;

R₃ represents hydrogen, halogen, cyano, nitro, mercapto, hydroxy, —C(═S)NH₂, —SF₅, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆ alkyl)amino, a 5-membered heterocycle containing 1-4 nitrogen atoms, piperidino, morpholino, thiomorpholino, formyl, hydroxycarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ haloalkenyloxycarbonyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl, C₁-C₆ hydroxyalkyl, phenyl or benzyl wherein the phenyl and benzyl are optionally substituted by one or more groups independently selected from the group consisting of halogen, cyano, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, methylamino and dimethylamino;

R₅ is hydrogen, C₁-C₁₂alkyl, C₃-C₁₂alkenyl, C₃-C₁₂alkynyl, C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl or benzylsulfonyl, or is C₁-C₁₂alkyl, C₂-C₁₂alkenyl, C₂-C₁₂alkynyl, C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl or benzylsulfonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, azido, formyl, C₂-C₇alkylcarbonyl, C₂-C₇haloalkylcarbonyl, C₁-C₆alkyl, C₁-C₆haloalkyl, C₁-C₆alkoxy, C₁-C₆haloalkoxy, C₁-C₆alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆alkylsulfonyl; or

R₅ is formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl, phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂ alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl or phenoxycarbonyl, or is C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl, phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂ alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl or phenoxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-, (R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—, (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein the group B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—, —ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)2-, —S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—, —C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₅cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, in turn, are mono- to poly-substituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, mercapto, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- or A-O—(C₃-C₈cycloalkyl)-;

wherein A is a three- to ten-membered monocyclic or fused bicyclic ring system which can be aromatic, partially saturated or fully saturated and can contain 1 to 4 hetero atoms selected from the group consisting of nitrogen, oxygen and sulphur, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the three- to ten-membered ring system to be itself mono- or polysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, azido, formyl, carboxy, ═O, ═S, C₁-C₆alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈ halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy, phenyl and phenoxy, in turn, may be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A2) by substituents independently selected form the group consisting of

(R₁₄)S(═O)(═NR₁₃)—, (R₁₄)(R₁₅)S(═O)═N—; —Si(R₅₁)(R₅₂)(R₅₃), —NR₅₇R₅₈, —C(═O)NR₅₇R₅₈, —C(═S)NR₅₇R₅₈, HC(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)—, (C₁-C₆haloalkyl)C(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)C₁-C₆alkyl-, (C₁-C₆haloalkyl)C(═NOR₅₉)C₁-C₆alkyl-, N(C₁-C₆alkyl)aminosulfonyl and N,N-di(C₁-C₆alkyl)aminosulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇ alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl, C₄-C₉ halocycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₃-C₇ alkenyloxycarbonyl, C₃-C₇ alkynyloxycarbonyl, C₄-C₉ cycloalkoxycarbonyl, C₂-C₇ alkylthiocarbonyl and benzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

A4) by substituents independently selected from the group consisting of hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl, ═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄ alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and ═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionally substituted by one or more group selected from the group consisting of halogen, methyl, halomethyl; or

R₅ is —N═C(R₈)(R₉); or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl, C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R₆ is selected from hydrogen and SH;

R₇ is hydrogen, halogen or C₁-C₄ alkyl;

R₈ and R₉, independently from each other, are hydrogen, halogen, cyano, C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, carboxy, C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl, or C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₈ and R₉ together from a C₂-C₈ alkylene bridge which may optionally be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, C₁-C₆ alkyl and C₁-C₆ haloalkyl; or R₈ and R₉, independently from each other, are the groups A-, A-O— or A-(C₁-C₆alkyl)-;

R₁₀ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl or C₁-C₄ haloalkyl;

R₁₃ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl, phenyl and benzyl, or is phenyl and benzyl mono- to polysubstituted by halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy;

R₁₄ and R₁₅, independently of each other, are C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl independently of each other, substituted by substituents selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;

R₅₁, R₅₂, R₅₃, independently of each other, are halogen, cyano, C₁-C₆ alkyl, C₂-C₆alkenyl, C₃-C₈ cycloalkyl, C₅-C₈ cycloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, benzyl or phenyl;

R₅₄, R₅₅, R₅₆, independently of each other, are C₁-C₆ alkyl, C₃-C₆ alkenyl, C₃-C₈ cycloalkyl, C₃-C₆ alkynyl, benzyl or phenyl;

R₅₇ and R₅₈, independently of each other, are hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl, phenyl or benzyl, where phenyl or benzyl for their part may be mono- to polysubstituted on the phenyl ring by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy, or R₅₇ and R₅₈ together with their interconnecting nitrogen atom are aziridino, azetidino, pyrazolino, pyrazolidino, pyrrolino, pyrrolidino, imidazolino, imidazolidino, triazolino, tetrazolino, piperazino, piperidino, morpholino, thiomorpholino, each of which, in turn, may be mono- or polysubstituted by substituents selected from the group consisting of methyl, halogen, cyano;

R₅₉ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl, benzyl and phenyl, and benzyl and phenyl mono- to polysubstituted by halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy;

R₆₀ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; R₆₂ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₃-C₆ alkenyl, C₃-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄ alkyl;

and agronomically acceptable salts/metallic complexes/metalloidic complexes/isomers/structural isomers/stereo-isomers/diastereoisomers/enantiomers/tautomers/N-oxides of those compounds; and

component B) is a strobilurin fungicide, a sterol biosynthesis inhibitor fungicide, a triazole fungicide, or a pro-triazole fungicide, or a DMI fungicide, or a SDHI fungicide, or a compound selected from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione, Sulcotrione, Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese, Cyflufenamid, Tebufloquin and Copper.

A further aspect of present invention provides a composition comprising a combination of components A) and B) in a synergistically effective ratio between the component A) and component B).

A further aspect of the present invention provides a method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components A) and B) in as synergistically effective amount and ratio between the component A) and component B).

A further aspect of the present invention relates to novel compounds according to formula (I).

A further aspect of the present invention relates to novel intermediates to provide compounds according to formula (I).

Preferably, component B is a strobilurin fungicide, a sterol biosynthesis inhibitor fungicide, a triazole fungicide, a pro-triazole fungicide, a DMI fungicide, a SDHI fungicide, or is a compound selected from Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Mefenoxam, Orocymedone, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione, Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese and Copper.

Preferably, component B is a strobilurin fungicide, a sterol biosynthesis inhibitor fungicide, a triazole fungicide, a pro-triazole fungicide, a DMI fungicide, a SDHI fungicide, or is a compound selected from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Mefenoxam, Orocymedone, Fluazinam, Carbendazim, Thiamethoxam, Glyphosate, 2,4-D, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol and cis-Jasmone.

In one group of mixtures, component B is a strobilurin fungicide.

In another group of mixtures, component B is a Sterol biosynthesis inhibitor

In another group of mixtures, component B is a triazole fungicide or a protriazole compound.

In another group of mixtures, component B is a DMI fungicide.

In another group of mixtures, component B is a SDHI fungicide.

In another group of mixtures, component B is a compound of formula (III)

wherein R^(70′) is phenyl, which is unsubstituted or substituted with 1, 2 or 3 substituents selected from halogen, haloalkyl, haloalkoxy and cyano, and;

R^(71′) is phenyl, which is unsubstituted or substituted with 1, 2 or 3 substituents selected from halogen, haloalkyl, haloalkoxy and cyano.

Preferred compounds of formula (III) are (S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol and 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.

In another group of mixtures, component B is selected from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione, Sulcotrione, Auxins (e.g. 2,4-D and MCPA), Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese and Copper, preferably from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Fenpropidin, Mandipropamid, Mefenoxam, Orocymedone, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione, Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese and Copper, more preferably from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Fenpropidin, Mandipropamid, Mefenoxam, Orocymedone, Fluazinam, Carbendazim, Thiamethoxam, Glyphosate, 2,4-D, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol and cis-Jasmone.

In a preferred embodiment the component B) is a compound selected from Chlorothalonil, Fludioxonil, Cyprodinil, Fenpropidin, Mandipropamid, Fenpropimorph, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, Acephat, Glyphosate, Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione, Sulcotrione, 2,4-D, MCPA, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese, Copper, Coumoxystrobin, Dicloaminostrobin, Flufenoxystrobin, Pyrametostrobin, Pyraoxystrobin, Trifloxystrobin, Azoxystrobin, Pyraclostrobin, Picoxystrobin, Jiaxiangjunzhi, Enoxastrobin, Triclopyricarb, the compound of formula II, Cyproconazole, Difenoconazole, Metconazole, Propiconazole, Epoxiconazole, Tebuconazole, Flutriafol, Ipconazole, prothioconazole, (S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol, 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol, Pyrisoxazole, 3-(Difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide, N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, Isopyrazam, Sedaxane, Boscalid, Fluxapyroxad, Penthiopyrad, Penflufen, Bixafen and Fluopyram.

The term strobilurin fungicide is well known to the person skilled in the art, and includes, for example, Coumoxystrobin, Dicloaminostrobin, Flufenoxystrobin, Pyrametostrobin, Pyraoxystrobin, Trifloxystrobin, Azoxystrobin, Pyraclostrobin, Picoxystrobin, Jiaxiangjunzhi, Enoxastrobin, Triclopyricarb, Fluoxastrobin, Dimoxystrobin, Fenaminostrobin and the compound of formula (II). Preferred strobilurin fungicides are Azoxystrobin, Pyraclostrobin and Picoxystrobin. Even more preferred strobilurin fungicides are Azoxystrobin and Pyraclostrobin.

The term sterol biosynthesis inhibitor fungicide is well known to the person skilled in the art, and includes, for example, Spiroxamine, Fenpropimorph, Tridemorph, Fenpropidin, Fenhexamid, Terbinafine, Naftifine

The term triazole fungicide is well known to the person skilled in the art, and includes, for example, Cyproconazole, Difenoconazole, Metconazole, Propiconazole, Epoxiconazole, Tebuconazole, Flutriafol, Ipconazole and 1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol [CAS number 120983-64-4]. Preferred triazole fungicide compounds are Cyproconazole, Difenoconazole, Metconazole and Tebuconazole. Even more preferred is Cyproconazole.

The term pro-triazole fungicide is well known to the person skilled in the art and includes, for example, prothioconazole.

The term DMI fungicides is well known to the person skilled in the art and includes, for example, (S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol, 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol and Pyrisoxazole. Preferred DMI fungicides are (S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol and 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.

The term SDHI fungicide is well known to the person skilled in the art and includes, for example, N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, Isopyrazam, Sedaxane, Boscalid Fluxapyroxad, Penthiopyrad, Penflufen, Bixafen, Fluopyram, 3-(Difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide, Preferred SDHI fungicides are N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, Isopyrazam, 3-(Difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide and Fluxapyroxad.

The term Auxins is well known to the person skilled in the art and includes, for example, 2,4-D, MCPA and Dicamba

In a further preferred embodiment the component B is Chlorothalonil. In a further preferred embodiment the component B is Fludioxonil. In a further preferred embodiment the component B is Cyprodinil. In a further preferred embodiment the component B is Fenpropidin. In a further preferred embodiment the component B is Mandipropamid. In a further preferred embodiment the component B is Fluazinam. In a further preferred embodiment the component B is Procymedone. In a further preferred embodiment the component B is Carbendazim. In a further preferred embodiment the component B is Abamectin. In a further preferred embodiment the component B is Clothianidin. In a further preferred embodiment the component B is Emamectin benzoate. In a further preferred embodiment the component B is Imidacloprid. In a further preferred embodiment the component B is Tefluthrin. In a further preferred embodiment the component B is Mefenoxam. In a further preferred embodiment the component B is Orocymedone. In a further preferred embodiment the component B is Thiamethoxam. In a further preferred embodiment the component B is Lambda-cyhalothrin. In a further preferred embodiment the component B is Gamma-cyhalothrin. In a further preferred embodiment the component B is Profenofos. In a further preferred embodiment the component B is Lufenuron. In a further preferred embodiment the component B is Diflubenzuron. In a further preferred embodiment the component B is Cypermethrin. In a further preferred embodiment the component B is Novaluron. In a further preferred embodiment the component B is Bifenthrin. In a further preferred embodiment the component B is Methomyl. In a further preferred embodiment the component B is Chlopyrifos. In a further preferred embodiment the component B is Methamidophos. In a further preferred embodiment the component B is Endosulfan. In a further preferred embodiment the component B is Betacyfluthrin. In a further preferred embodiment the component B is Triflumuron. In a further preferred embodiment the component B is Teflubenzuron. In a further preferred embodiment the component B is Acephat. In a further preferred embodiment the component B is Glyphosate. In a further preferred embodiment the component B is Glufosinate. In a further preferred embodiment the component B is Mesotrione. In a further preferred embodiment the component B is Bicyclopyrone. In a further preferred embodiment the component B is Tembotrione. In a further preferred embodiment the component B is Sulcotrione. In a further preferred embodiment the component B is 2,4-D. In a further preferred embodiment the component B is MCPA. In a further preferred embodiment the component B is Trinexapac-ethyl. In a further preferred embodiment the component B is Prohexadione-Ca. In a further preferred embodiment the component B is Paclobutrazol. In a further preferred embodiment the component B is Acibenzolar-S-methyl. In a further preferred embodiment the component B is Methyl-Jasmonate. In a further preferred embodiment the component B is Cis-Jasmone. In a further preferred embodiment the component B is Manganese. In a further preferred embodiment the component B is Copper. In a further preferred embodiment the component B is Cyflufenamid. In a further preferred embodiment the component B is Tebufloquin. In a further preferred embodiment the component B is Coumoxystrobin. In a further preferred embodiment the component B is Dicloaminostrobin. In a further preferred embodiment the component B is Flufenoxystrobin. In a further preferred embodiment the component B is Pyrametostrobin. In a further preferred embodiment the component B is Pyraoxystrobin. In a further preferred embodiment the component B is Trifloxystrobin. In a further preferred embodiment the component B is Azoxystrobin. In a further preferred embodiment the component B is Pyraclostrobin. In a further preferred embodiment the component B is Picoxystrobin. In a further preferred embodiment the component B is Jiaxiangjunzhi. In a further preferred embodiment the component B is Enoxastrobin. In a further preferred embodiment the component B is Triclopyricarb. In a further preferred embodiment the component B is Fluoxastrobin. In a further preferred embodiment the component B is Dimoxystrobin. In a further preferred embodiment the component B is Fenaminostrobin In a further preferred embodiment the component B is the compound of formula II. In a further preferred embodiment the component B is Cyproconazole. In a further preferred embodiment the component B is Difenoconazole. In a further preferred embodiment the component B is Metconazole. In a further preferred embodiment the component B is Propiconazole. In a further preferred embodiment the component B is Epoxiconazole. In a further preferred embodiment the component B is Tebuconazole. In a further preferred embodiment the component B is Flutriafol. In a further preferred embodiment the component B is Ipconazole. In a further preferred embodiment the component B is 1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol [CAS number 120983-64-4]. In a further preferred embodiment the component B is prothioconazole. In a further preferred embodiment the component B is (S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol. In a further preferred embodiment the component B is 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol. In a further preferred embodiment the component B is Pyrisoxazole. In a further preferred embodiment the component B is 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-Pyrazole-4-carboxamide. In a further preferred embodiment the component B is N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide. In a further preferred embodiment the component B is Isopyrazam. In a further preferred embodiment the component B is Sedaxane. In a further preferred embodiment the component B is Boscalid, In a further preferred embodiment the component B is Fluxapyroxad. In a further preferred embodiment the component B is Penthiopyrad. In a further preferred embodiment the component B is Penflufen. In a further preferred embodiment the component B is Bixafen. In a further preferred embodiment the component B is Fluopyram. In a further preferred embodiment the component B is 1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol.

The active ingredient mixture according to the invention may bring about the additive enhancement of the spectrum of action with respect to the phytopathogen to be controlled that may in principle be expected but achieves a synergistic effect which extends the range of action of the component (A) and of the component (B) in two ways. Firstly, the rates of application of the component (A) and of the component (B) may be lowered whilst the action remains equally good. Secondly, the active ingredient mixture may still achieve a high degree of phytopathogen control even where the two individual components have become totally ineffective in such a low application rate range. This allows, on the one hand, a substantial broadening of the spectrum of phytopathogens that can be controlled and, on the other hand, increased safety in use.

However, besides the actual synergistic action with respect to fungicidal activity, the pesticidal compositions according to the invention may also have further surprising advantageous properties which can also be described, in a wider sense, as synergistic activity. Examples of such advantageous properties that may be mentioned are: a broadening of the spectrum of fungicidal activity to other phytopathogens, for example to resistant strains; a reduction in the rate of application of the active ingredients; synergistic activity against animal pests, such as insects or representatives of the order Acarina; a broadening of the spectrum of pesticidal activity to other animal pests, for example to resistant animal pests; adequate pest control with the aid of the compositions according to the invention, even at a rate of application at which the individual compounds are totally ineffective; advantageous behaviour during formulation and/or upon application, for example upon grinding, sieving, emulsifying, dissolving or dispensing; increased storage stability; improved stability to light; more advantageous degradability; improved toxicological and/or ecotoxicological behaviour; improved characteristics of the useful plants including: emergence, crop yields, more developed root system, tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf colour, less fertilizers needed, less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, improved plant vigor, and early germination; or any other advantages familiar to a person skilled in the art.

Substituents at a nitrogen atom are always different from halogen. A hydroxy, mercapto or amino substituent is not to be placed on an α-carbon relative to a heteroatom of a core fragment.

The alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl, hexyl, heptyl and octyl and their branched isomers. Alkoxy, alkenyl and alkynyl radicals are derived from the alkyl radicals mentioned. The alkenyl and alkynyl groups can be mono- or polyunsaturated.

The cycloalkyl groups occurring in the definitions of the substituents are, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.

Halogen is generally fluorine, chlorine, bromine or iodine, preferably fluorine, bromine or chlorine. This also applies, correspondingly, to halogen in combination with other meanings, such as haloalkyl or haloalkoxy.

Haloalkyl groups preferably have a chain length of from 1 to 6 carbon atoms. Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl, 2,2,2-trichloroethyl, 5,5,5-trifluoropentan-1-yl, 5,5-difluoro-pentan-1-yl, 6,6,6-trifluorohexan-1-yl, 6,6-difluoro-hexan-1-yl, heptafluoro-prop-2-yl and 2-fluoro-prop-2-yl; preferably trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.

Suitable haloalkenyl groups are alkenyl groups which are mono- di- or trisubstituted by halogen, halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1-methylvinyl, 3-fluoropropenyl, 3-chloropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3-trichloropropenyl and 4,4,4-trifluorobut-2-en-1-yl.

Suitable haloalkynyl groups are, for example, alkynyl groups which are mono- or polysubstituted by halogen, halogen being bromine, iodine and in particular fluorine and chlorine, for example 3-fluoropropynyl, 3-chloropropynyl, 3-bromopropynyl, 3,3,3-trifluoro-propynyl and 4,4,4-trifluorobut-2-yn-1-yl.

Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy; preferably methoxy and ethoxy. Halogenalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy and trifluoromethoxy.

Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl. Haloalkoxy groups preferably have a chain length of from 1 to 6 carbon atoms. Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy and trifluoromethoxy. Alkylthio groups preferably have a chain length of from 1 to 6 carbon atoms.

Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl.

Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio. Alkylsulfinyl is, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl, tert-butylsulfinyl; preferably methylsulfinyl and ethylsulfinyl. Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl or ethylsulfonyl.

C₂-C₆ alkylcarbonyl is, for example, methylcarbonyl, ethylcarbonyl, propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, tert-butylcarbonyl or n-pentylcarbonyl and their branched isomers, preferably methylcarbonyl and ethylcarbonyl. Haloalkylcarbonyl radicals are derived from the alkyl radicals mentioned.

In the context of the present invention “mono- to polysubstituted” in the definition of the substituents, means typically, depending on the chemical structure of the substituents, monosubstituted to seven-times substituted, preferably monosubstituted to five-times substituted, more preferably mono-, double- or triple-substituted.

According to the present invention, a three- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic, partially saturated or fully saturated is, depending of the number of ring members, for example, selected from the group consisting of

cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, where said cycloalkylgroups for their part may be preferably unsubstituted or substituted by C₁-C₆alkyl or halogen, or is phenyl, benzyl, naphthyl or the following heterocyclic groups: pyrrolyl; pyridyl; pyrazolyl; pyrimidyl; pyrazinyl; imidazolyl; thiadiazolyl; quinazolinyl; furyl; oxadiazolyl; indolizinyl; pyranyl; isobenzofuranyl; thienyl; naphthyridinyl; (1-methyl-1H-pyrazol-3-yl)-; (1-ethyl-1H-pyrazol-3-yl)-; (1-propyl-1H-pyrazol-3-yl)-; (1H-pyrazol-3-yl)-; (1,5-dimethyl-1H-pyrazol-3-yl)-; (4-chloro-1-methyl-1H-pyrazol-3-yl)-; (1H-pyrazol-1-yl)-; (3-methyl-1H-pyrazol-1-yl)-; (3,5-dimethyl-1H-pyrazol-1-yl)-; (3-isoxazolyl)-; (5-methyl-3-isoxazolyl)-; (3-methyl-5-isoxazolyl)-; (5-isoxazolyl)-; (1H-pyrrol-2-yl)-; (1-methyl-1H-pyrrol-2-yl)-; (1H-pyrrol-1-yl)-; (1-methyl-1H-pyrrol-3-yl)-; (2-furanyl)-; (5-methyl-2-furanyl)-; (3-furanyl)-; (5-methyl-2-thienyl)-; (2-thienyl)-; (3-thienyl)-; (1-methyl-1H-imidazol-2-yl)-; (1H-imidazol-2-yl)-; (1-methyl-1H-imidazol-4-yl)-; (1-methyl-1H-imidazol-5-yl)-; (4-methyl-2-oxazolyl)-; (5-methyl-2-oxazolyl)-; (2-oxazolyl)-; (2-methyl-5-oxazolyl)-; (2-methyl-4-oxazolyl)-; (4-methyl-2-thiazolyl)-; (5-methyl-2-thiazolyl)-; (2-thiazolyl)-; (2-methyl-5-thiazolyl)-; (2-methyl-4-thiazolyl)-; (3-methyl-4-isothiazolyl)-; (3-methyl-5-isothiazolyl)-; (5-methyl-3-isothiazolyl)-; (1-methyl-1H-1,2,3-triazol-4-yl)-; (2-methyl-2H-1,2,3-triazol-4-yl)-; (4-methyl-2H-1,2,3-triazol-2-yl)-; (1-methyl-1H-1,2,4-triazol-3-yl)-; (1,5-dimethyl-1H-1,2,4-triazol-3-yl)-; (3-methyl-1H-1,2,4-triazol-1-yl)-; (5-methyl-1H-1,2,4-triazol-1-yl)-; (4,5-dimethyl-4H-1,2,4-triazol-3-yl)-; (4-methyl-4H-1,2,4-triazol-3-yl)-; (4H-1,2,4-triazol-4-yl)-; (5-methyl-1,2,3-oxadiazol-4-yl)-; (1,2,3-oxadiazol-4-yl)-; (3-methyl-1,2,4-oxadiazol-5-yl)-; (5-methyl-1,2,4-oxadiazol-3-yl)-; (4-methyl-3-furazanyl)-; (3-furazanyl)-; (5-methyl-1,2,4-oxadiazol-2-yl)-; (5-methyl-1,2,3-thiadiazol-4-yl)-; (1,2,3-thiadiazol-4-yl)-; (3-methyl-1,2,4-thiadiazol-5-yl)-; (5-methyl-1,2,4-thiadiazol-3-yl)-; (4-methyl-1,2,5-thiadiazol-3-yl)-; (5-methyl-1,3,4-thiadiazol-2-yl)-; (1-methyl-1H-tetrazol-5-yl)-; (1H-tetrazol-5-yl)-; (5-methyl-1H-tetrazol-1-yl)-; (2-methyl-2H-tetrazol-5-yl)-; (2-ethyl-2H-tetrazol-5-yl)-; (5-methyl-2H-tetrazol-2-yl)-; (2H-tetrazol-2-yl)-; (2-pyridyl)-; (6-methyl-2-pyridyl)-; (4-pyridyl)-; (3-pyridyl)-; (6-methyl-3-pyridazinyl)-; (5-methyl-3-pyridazinyl)-; (3-pyridazinyl)-; (4,6-dimethyl-2-pyrimidinyl)-; (4-methyl-2-pyrimidinyl)-; (2-pyrimidinyl)-; (2-methyl-4-pyrimidinyl)-; (2-chloro-4-pyrimidinyl)-; (2,6-dimethyl-4-pyrimidinyl)-; (4-pyrimidinyl)-; (2-methyl-5-pyrimidinyl)-; (6-methyl-2-pyrazinyl)-; (2-pyrazinyl)-; (4,6-dimethyl-1,3,5-triazin-2-yl)-; (4,6-dichloro-1,3,5-triazin-2-yl)-; (1,3,5-triazin-2-yl)-; (4-methyl-1,3,5-triazin-2-yl)-; (3-methyl-1,2,4-triazin-5-yl)-; (3-methyl-1,2,4-triazin-6-yl)-;

wherein each R₂₆ is methyl, each R₂₇ and each R₂₈ are independently hydrogen, C₁-C₃alkyl, C₁-C₃alkoxy, C₁-C₃alkylthio or trifluoromethyl, X₄ is oxygen or sulfur and r=1, 2, 3 or 4.

There no free valency is indicated in those definitions, for example as in

the linkage site is located at the carbon atom labelled “CH” or in a case such as, for example,

at the bonding site indicated at the bottom left.

The following substituents definitions, including preferred definitions, may be combined in any combination:

R₁ and R₂ are each independently selected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl, C₃-C₄ alkynyl, (R₁₀)carbonyl and (R₁₀)oxycarbonyl;

-   -   or R₁ and R₂ together with the nitrogen atom to which they are         attached form a 5- or 6 membered cyclic group which may be         saturated or unsaturated and may contain a further heteroatom         selected from S or O.

Preferably, R₁ and R₂ are each independently selected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₃-C₄ alkynyl;

or R₁ and R₂ together with the nitrogen atom to which they are attached form a pyrrolidine or piperidine.

More preferably, R₁ and R₂ are each independently selected from hydrogen or C₁-C₄ alkyl;

or R₁ and R₂ together with the nitrogen atom to which they are attached form a pyrrolidine or piperidine.

Even more preferably, R₁ and R₂ are each independently selected from hydrogen or C₁-C₄ alkyl.

More preferably again, R₁ and R₂ are each C₁-C₄ alkyl.

More favourably again, R₁ and R₂ are each independently selected from methyl, ethyl and isopropyl.

Yet more favourably, R₁ is methyl and R₂ is selected from methyl, ethyl and isopropyl.

Yet more favourably still, R₁ is methyl and R₂ is selected from ethyl and isopropyl.

Most preferably, R₁ is methyl and R₂ is ethyl.

R₃ represents hydrogen, halogen, cyano, nitro, mercapto, hydroxy, —C(═S)NH₂, —SF₅, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆cycloalkyl, amino, C₁-C₂alkylamino, di(C₁-C₆alkyl)amino, a 5-membered heterocycle containing 1-4 nitrogen atoms, piperidino, morpholino, thiomorpholino, formyl, hydroxycarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ haloalkenyloxycarbonyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl, C₁-C₆ hydroxyalkyl, phenyl or benzyl wherein the phenyl and benzyl are optionally substituted by one or more groups independently selected from the group consisting of halogen, cyano, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl.

Preferably, R₃ represents hydrogen, halogen, cyano, mercapto, hydroxy, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ haloalkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, tetrazolino, formyl, C₂-C₅ alkylcarbonyl, C₂-C₅ haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl or C₁-C₆ hydroxyalkyl.

More preferably, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, formyl, phenyl, C₂-C₄ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl or C₁-C₆ hydroxyalkyl.

Even more preferably, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, formyl, C₂-C₄alkylcarbonyl, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄ haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl or C₁-C₆ hydroxyalkyl.

More preferably again, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄ alkylsulfonyl.

Favourably, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄ alkylsulfonyl.

Even more favourably, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy or C₃-C₆ cycloalkyl.

More favourably again, R₃ represents hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, cyclopropyl, ethynyl or C₁-C₄ alkoxy.

Yet more favourably, R₃ is selected from hydrogen, bromine, iodine, methyl, CHF₂, cyclopropyl, ethynyl and methoxy.

Yet more favourably still, R₃ represents hydrogen, bromine, iodine, methyl, difluoromethyl or methoxy.

Most preferably, R₃ represents bromine or methyl.

R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, methylamino or dimethylamino.

Preferably, R₄ is selected from hydrogen, fluorine, chlorine, bromine, C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₃-C₆ cycloalkyl.

More preferably, R₄ is selected from fluorine, chlorine, bromine, C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₃-C₆ cycloalkyl.

Even more preferably, R₄ is selected from fluorine, chlorine, methyl, ethyl, ethenyl, propyl, propenyl, isopropyl, isopropenyl, cyclopropanyl, methoxy, ethoxy, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoromethyl.

More preferably again, R₄ is selected from methyl, ethyl, methoxy, fluorine and chlorine.

More favourably again, R₄ is selected from methyl, methoxy, fluorine and chlorine.

Most preferably, R₄ is methyl.

In another group of compounds, R₄ is selected from methoxy, fluorine and chlorine.

R₅ is hydrogen, C₁-C₁₂alkyl, C₃-C₁₂alkenyl, C₃-C₁₂alkynyl, C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl or benzylsulfonyl, or is C₁-C₁₂alkyl, C₂-C₁₂alkenyl, C₂-C₁₂alkynyl, C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl or benzylsulfonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, azido, formyl, C₂-C₇alkylcarbonyl, C₂-C₇haloalkylcarbonyl, C₁-C₆alkyl, C₁-C₆haloalkyl, C₁-C₆alkoxy, C₁-C₆haloalkoxy, C₁-C₆alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆alkylsulfonyl; or

R₅ is formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl, phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂alkenyloxycarbonyl, C₄-C₁₂ alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl or phenoxycarbonyl, or is C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl, phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂ alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl or phenoxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-, (R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—, (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein the group B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—, —ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)₂—, —S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—, —C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, in turn, are mono- to poly-substituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, mercapto, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- or A-O—(C₃-C₈cycloalkyl)-; or

wherein A is a three- to ten-membered monocyclic or fused bicyclic ring system which can be aromatic, partially saturated or fully saturated and can contain 1 to 4 hetero atoms selected from the group consisting of nitrogen, oxygen and sulphur, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the three- to ten-membered ring system to be itself mono- or polysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy, ═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈ halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy, phenyl and phenoxy, in turn, may be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A2) by substituents independently selected form the group consisting of (R₁₄)S(═O)(═NR₁₃)—, (R₁₄)(R₁₅)S(═O)═N—; —Si(R₅₁)(R₅₂)(R₅₃), —NR₅₇R₅₈, —C(═O)NR₅₇R₅₈, —C(═S)NR₅₇R₅₈, HC(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)—, (C₁-C₆haloalkyl)C(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)C₁-C₆alkyl-, (C₁-C₆haloalkyl)C(═NOR₅₉)C₁-C₆alkyl-, N(C₁-C₆alkyl)aminosulfonyl and N,N-di(C₁-C₆alkyl)aminosulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇ alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl, C₄-C₉ halocycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₃-C₇ alkenyloxycarbonyl, C₃-C₇ alkynyloxycarbonyl, C₄-C₉ cycloalkoxycarbonyl, C₂-C₇ alkylthiocarbonyl and benzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or A4) by substituents independently selected from the group consisting of hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl, ═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄ alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and ═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionally substituted by one or more group selected from the group consisting of halogen, methyl, halomethyl; or

R₅ is —N═C(R₈)(R₉); or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl, C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂.

Preferably, R₅ represents hydrogen, C₁-C₁₂ alkylsulfonyl, C₁-C₁₂ alkyl, C₃-C₁₂ alkenyl, C₃-C₁₂ alkynyl, or is C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, azido, formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-, (R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—, (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein the group B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—, —ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)₂—, —S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—, —C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, in turn, are mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, mercapto, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is selected from A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- and A-O—(C₃-C₈cycloalkyl)-;

wherein A is a three- to ten-membered monocyclic or fused bicyclic ring system which can be aromatic, partially saturated or fully saturated and can contain 1 to 4 hetero atoms selected from the group consisting of nitrogen, oxygen and sulphur, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the three- to ten-membered ring system to be itself mono- or polysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy, ═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈ halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, C₃-C₈ halocycloalkyloxy, C₃-C₈ cycloalkenyloxy, C₃-C₈ halocycloalkenyloxy, benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy, phenyl and phenoxy, in turn, may be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇ alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₄-C₉ cycloalkoxycarbonyl and benzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

A4) by substituents independently selected from the group consisting of hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl, ═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄ alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and ═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionally substituted by one or more group selected from the group consisting of halogen, methyl, halomethyl; or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl, C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂.

More preferably, R₅ is selected from G¹, G², G³-G⁴, G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹², G¹³, G¹⁴, G¹⁵ and G¹⁶.

More preferably again, R₅ is selected from G¹, G², G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹², G¹⁴, G¹⁵ and G¹⁶.

More favourably again, R₅ is selected from G², G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹⁴ and G¹⁶.

Most preferably, R₅ is selected from G², G⁵, G⁸ and G¹⁰-G¹¹.

R₆ is selected from hydrogen and SH.

Most preferably, R₆ is hydrogen.

In one group of compounds, R₆ is SH.

R₇ is hydrogen, halogen or C₁-C₄ alkyl.

Preferably, R₇ is hydrogen or C₁-C₄ alkyl.

Most preferably, R₇ is hydrogen.

R₈ and R₉, independently from each other, are hydrogen, halogen, cyano, C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, carboxy, C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl, or C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₈ and R₉ together from a C₂-C₈ alkylene bridge which may optionally be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, C₁-C₆ alkyl and C₁-C₆ haloalkyl; or R₈ and R₉, independently from each other, are the groups A-, A-O— or A-(C₁-C₆alkyl)-.

R₁₀ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl or C₁-C₄ haloalkyl.

R₁₃ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl, phenyl and benzyl, or is phenyl and benzyl mono- to polysubstituted by halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy.

R₁₄ and R₁₅, independently of each other, are C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl independently of each other, substituted by substituents selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy.

R₅₁, R₅₂, R₅₃, independently of each other, are halogen, cyano, C₁-C₆ alkyl, C₂-C₆alkenyl, C₃-C₈ cycloalkyl, C₅-C₈ cycloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, benzyl or phenyl.

R₅₄, R₅₅, R₅₆, independently of each other, are C₁-C₆ alkyl, C₃-C₆ alkenyl, C₃-C₈ cycloalkyl, C₃-C₆ alkynyl, benzyl or phenyl.

R₅₇ and R₅₈, independently of each other, are hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl, phenyl or benzyl, where phenyl or benzyl for their part may be mono- to polysubstituted on the phenyl ring by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy, or R₅₇ and R₅₈ together with their interconnecting nitrogen atom are aziridino, azetidino, pyrazolino, pyrazolidino, pyrrolino, pyrrolidino, imidazolino, imidazolidino, triazolino, tetrazolino, piperazino, piperidino, morpholino, thiomorpholino, each of which, in turn, may be mono- or polysubstituted by substituents selected from the group consisting of methyl, halogen, cyano.

R₅₉ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl, benzyl and phenyl, and benzyl and phenyl mono- to polysubstituted by halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy.

R₆₀ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;

R₆₂ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₃-C₆ alkenyl, C₃-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy.

G¹ is a C₈-C₁₀ fused bicyclic ring system which may be saturated or comprise one carbon-carbon double bond and is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano.

More preferably, G¹ is a C₉-C₁₀ fused bicyclic ring system which may be saturated or comprise one carbon-carbon double bond and is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano.

More preferably again, G¹ is a C₉-C₁₀ fused bicyclic ring system which may be saturated or comprise one carbon-carbon double bond and is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl.

More favourably, G¹ is a saturated C₉-C₁₀ fused bicyclic ring system which is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, fluoro, methoxy and C₁-C₄ fluoroalkyl.

More favourably again, G¹ is a saturated C₁₀ fused bicyclic ring system which is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl.

Most preferably, G¹ is a saturated C₁₀ fused bicyclic ring system.

G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

More preferably again, G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or more groups independently selected from halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio.

Favourably, G² is C₅-C₆ cycloalkenyl, which is optionally substituted by one or more groups independently selected from halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl and C₁-C₆ alkoxy.

More favourably, G² is a C₅-C₆ cycloalkenyl group optionally substituted by one or more groups independently selected from fluorine, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl.

More favourably again, G² is a C₅-C₆ cycloalkenyl group optionally substituted by one or more fluorine atoms.

Most preferably, G² is a C₅-C₆ cycloalkenyl group.

In one group of compounds, G² is a C₅-C₆ cycloalkenyl group optionally substituted one or more groups selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl and C₁-C₆ alkoxy.

Preferably in this group of compounds, G² is a C₅-C₆ cycloalkenyl group optionally substituted one or more groups selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl.

G³ is phenyl, which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionally substituted by one or more halogen.

More preferably again, G³ is phenyl, which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ fluoroalkyl, C₁-C₄ alkoxy and halogen.

More favourably again, G³ is phenyl, which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, CHF₂, CF₃, C₁-C₄ alkoxy and halogen.

Yet more favourably, G³ is phenyl, which is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, CHF₂, CF₃, C₁-C₄ alkoxy and halogen.

Most preferably, G³ is phenyl.

G⁴ is C₃-C₁₂ cycloalkyl which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionally substituted by one or more halogen.

More preferably again, G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionally substituted by one or more halogen.

More favourably again, G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy and halogen.

Yet more favourably, G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, C₁-C₄ alkoxy and halogen.

Yet more favourably still, G⁴ is cyclohexyl or cyclopentyl.

Most preferably, G⁴ is cyclohexyl.

G⁵ is C₃-C₇ cycloalkyl, which is optionally substituted by one or more groups independently selected from halogen, ON, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆-alkenyloxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, phenoxy, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂.

More preferably, G⁵ is C₃-C₇ cycloalkyl, which is optionally substituted by one or more groups independently selected from halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy, C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio.

More preferably again, G⁵ is C₃-C₇ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—OH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy, C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio.

More preferably still, G⁵ is C₅-C₇ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—OH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₄ alkoxy, C₃-C₄-alkenyloxy, phenoxy and C₂-C₆ haloalkyl.

More favourably again, G⁵ is C₅-C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂ and C₂-C₆ haloalkyl.

Yet more favourably, G⁵ is C₅-C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂—CH(CH₃)—CH(CH₃)₂, CHF₂ and CF₃.

Most preferably, G⁵ is C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂ and —CH(CH₃)—CH(CH₃)₂.

In another group of compounds, G⁵ is a C₅-C₆ cycloalkyl, which is optionally substituted by one or more halogen.

More preferably in this group, G⁵ is a C₅-C₆ cycloalkyl, which is optionally substituted by one or more fluorine.

Even more preferably in this group, G⁵ is an unsubstituted C₅-C₆ cycloalkyl.

In another group of compounds, G⁵ is a C₅-C₆ cycloalkyl, which is optionally substituted by one or more groups selected from the group consisting of C₁-C₄ alkoxy, C₃-C₄-alkenyloxy or phenoxy.

Preferably in this group of compounds, G⁵ is a C₅-C₆ cycloalkyl, which is optionally substituted by one or more groups selected from the group consisting of methoxy, ethoxy, C₃-C₄ alkenyloxy and phenoxy.

G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, ON, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably again, G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, ON, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl.

Yet more preferably, G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, CN, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy and C₁-C₆ alkylthio.

Favourably, G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, ON, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy.

More favourably again, G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy.

Yet more favourably, G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more halogen, CHF₂, CF₃ and C₁-C₄ alkyl.

Most preferably, G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more methyl, bromine, iodine or chlorine.

In one group of compounds, G⁶ is phenyl substituted at the para-position by fluorine and further substituted as in the above paragraphs.

In one group of compounds, G⁶ is phenyl substituted at the ortho-position by fluorine and further substituted as in the above paragraphs.

In one group of compounds, G⁶ is phenyl substituted at the meta-position by fluorine and further substituted as in the above paragraphs.

G⁷ is methylene.

G⁸ is

G⁹ is

G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylsulfonyl, phenyl, 2-phenyl-ethynyl and 2-phenyl-ethyl.

Preferably, G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably, G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, OH, SH, CHO, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl.

More preferably again, G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, phenyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃.

More favourably again, G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, OH, methyl, ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, phenyl, ethoxy, iso-propyloxy and OCHF₂.

Yet more favourably, G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, ethenyl, methoxy, ethoxy, iso-propyloxy, phenyl, CHF₂, CF₃, CHF—CH₃ and OCHF₂.

Most preferably, G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, ethenyl, methoxy, phenyl, CHF₂, CF₃ and CHF—CH₃.

G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy.

More preferably again, G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy.

More favourably again, G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy.

Yet more favourably, G¹¹ is methylene substituted by at least one group independently selected from methyl, ethyl, CHF₂ and CF₃.

More favourably still, G¹¹ is methylene substituted by at least one group independently selected from methyl, CF₃ and ethyl.

Most preferably, G¹¹ is methylene substituted by at least one group independently selected from methyl and ethyl.

G¹² is

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂.

More preferably again, G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O.

Most preferably, G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy and ═O.

G¹⁴ is

G¹⁵ is

G¹⁶ is

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 to 4 members selected from the group consisting of N, N(R^(69′)), O and S (for example, pyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazole or tetrazole), it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More favourably again, G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 to 4 members selected from the group consisting of N, N(R^(69′)), O and S, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzyl are optionally substituted by halogen, CN, C₁-C₄ alkyl or C₁-C₄ haloalkyl.

Yet more favourably, G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 or 2 members selected from the group consisting of N, N(R^(69′)), O and S, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzyl are optionally substituted by halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl.

Most preferably, G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 or 2 members selected from the group consisting of N, O and S, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl.

In one group of compounds, G¹⁷ is selected from pyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazole or tetrazole each of which may be substituted by one or more groups selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More favourably again in this group, G¹⁷ is selected from pyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazole or tetrazole each of which may be substituted by one or more groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzyl are optionally substituted by halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl.

Yet more favourably in this group, G¹⁷ is selected from pyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, or imidazole each of which may be substituted by one or more groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzyl are optionally substituted by halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl.

Most preferably in this group, G¹⁷ is selected from pyridine, furan, pyrrole, thiazole or oxazole or imidazole each of which may be substituted by one or more groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl.

In another group of compounds, G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 member selected from the group consisting of N and O (for example, pyridine, furan or pyrrole), it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy or C₁-C₄ haloalkoxy.

Preferably in this group, G¹⁷ is pyridine, furan or pyrrole each of which may be mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy or C₁-C₄ haloalkoxy.

In another group of compounds, G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 2 members selected from the group consisting of N, O and S, (for example oxazole or thiazole) it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl.

Preferably in this group, G¹⁷ is oxazole or thiazole each of which may be mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl.

R^(1′) is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio.

More preferably again, R^(1′) is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl and C₁-C₄ fluoroalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio.

Yet more preferably, R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, methoxy, ethoxy and S—CH₃ S—CH₂CH₃.

More favourably again, R^(1′) is selected from the group consisting of hydrogen, fluorine, methyl, CH₂F and CF₃;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, methyl, CH₂F, CF₃ and methoxy.

Most preferably, R¹, R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen.

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably again, R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, cyano, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio.

More favourably again, R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂, CF₃ and C₁-C₄ alkoxy.

Most preferably, R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ alkoxy.

R^(15′) and R^(16′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio.

More preferably again, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are independently selected from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃ and CF₂CF₃;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio.

Favourably, R^(15′), R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are independently selected from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio.

More favourably, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are each independently selected from hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂ and CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio.

More favourably again, R^(15′), R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R²¹ and R²² are each independently selected from hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, methyl, fluorine, chlorine, bromine, ethyl, CH₂F, CHF₂ and CF₃ and isopropyl.

Yet more favourably, R^(15′), R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each independently selected from hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are each independently selected from hydrogen, fluorine, chlorine, bromine, methyl, ethyl and isopropyl.

Most preferably, R^(15′), R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′), R^(22′), R^(23′), R^(24′) and R^(25′) are each independently selected from hydrogen, methyl, ethyl and isopropyl.

In one group of compounds, R^(15′) and R^(16′) are each independently selected from the group consisting of hydrogen, methyl, F and CF₃.

In this group, R^(15′), R¹⁶, R¹⁷, R^(18′), R^(19′), R²⁰, R²¹ and R²² are most preferably each hydrogen.

In another preferred group of compounds, R^(15′) is as described above and R¹⁶, R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are each hydrogen.

In another group of compounds, R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, fluorine, chlorine, bromine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃.

R^(26′) is C(R^(36′))₂, N—OH, N—O—C₁-C₄-alkyl, N—O—C₂-C₄-alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O wherein the N—O-benzyl and N—O-phenyl may be substituted by one or more groups independently selected from the group consisting of halogen, methyl and halomethyl.

Most preferably, R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O or C(R³⁶).

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selected from the group consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl and phenyl;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond.

More preferably again, R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selected from the group consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond.

More favourably again, R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selected from the group consisting of hydrogen, C₁-C₄ alkyl and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond.

Yet more favourably R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each hydrogen or methyl;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond.

Most preferably R²⁷ is hydrogen or methyl;

R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each hydrogen; or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond.

Each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄ alkyl.

R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio.

More preferably again, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from a group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl.

Favourably, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from a group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂, and CH₂—CF₃.

More favourably again, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are independently selected from the group consisting of hydrogen, fluorine, methyl and trifluoromethyl.

Yet more favourably, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are hydrogen or methyl.

Most preferably, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are hydrogen.

In one group of compounds, R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen, and R^(37′) is as defined above.

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably again, R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected from the group consisting of hydrogen, fluorine, chlorine, bromine, iodine, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, methlythio, methylsulfinyl and methylsulfonyl.

Most preferably, R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected from the group consisting of hydrogen, fluorine, chlorine, methyl, CF₃, CHF₂, CH₂F, methoxy, difluoromethoxy and trifluoromethoxy.

R^(50′) is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄ alkylthio.

More preferably again, R^(50′), is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄ haloalkoxy.

Favourably, R^(50′), R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃, CHF—CH₃ and CF₂—CH₃.

More favourably again, R⁵⁰, R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, methyl, CH₂F and CF₃.

Most preferably, R⁵⁰, R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are each hydrogen.

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxy, C₂-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

More preferably again, R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, cyano, halogen, C₁-C₆ alkyl and C₁-C₆ haloalkyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

More favourably again, R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂ and CF₃; provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

Most preferably, R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen and halogen;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

In another group of compounds, R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, phenyl and halophenyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

In another group of compounds, R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, methy, ethyl and hydroxy-C₂-C₄-alkyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

Preferably in this group, R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen and hydroxyethyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen.

R^(61′) and R^(62′) are selected independently of each other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio.

More preferably again, R^(61′) and R^(62′) are selected independently of each other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(63′), R^(64′), R^(65′), R⁶⁶, R⁶⁷ and R^(68′) are selected independently of each other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy.

More favourably again, R^(61′) and R^(62′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, CHF₂ and CF₃;

R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, methoxy, difluoromethoxy, trifluoromethoxy, CHF₂ and CF₃.

Yet more favourably, R^(61′), R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are hydrogen, CHF₂, CF₃ or methyl.

Yet more favourably still, R^(61′), R^(62′), R⁶³, R⁶⁴, R⁶⁵, R⁶⁶, R⁶⁷ and R⁶⁸ are hydrogen or methyl.

Most preferably, R^(61′), R⁶², R⁶³, R⁶⁴, R⁶⁵, R⁶⁶, R⁶⁷ and R⁶⁸ are hydrogen.

R^(69′) is selected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₁-C₄ alkylcarboxy.

More preferably again, R^(69′) is selected from hydrogen, C₁-C₄ alkyl and C₁-C₄ alkylcarboxy.

More favourably again, R^(69′) is selected from hydrogen and C₁-C₄ alkyl.

Most preferably, R^(69′) is hydrogen.

n is 0 or 1.

In one preferred group of compounds, n is 0.

In another preferred group of compounds, n is 1.

p and q are independently selected from 0 and 1.

In one group of compounds, p and q are 0.

In another group of compounds, p and q are 1.

In another group of compounds, p is 1 and q is 0.

r, s and t are independently selected from 0 and 1.

More preferably again, r and s are 0 and t is 1 or 0.

Most preferably, r, s and t are each 0.

In a group of compounds of formula I, R₁ and R₂ are each independently selected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₃-C₄ alkynyl;

or R₁ and R₂ together with the nitrogen atom to which they are attached form a pyrrolidine or piperidine;

R₃ represents hydrogen, halogen, cyano, mercapto, hydroxy, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ haloalkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkyl amino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, tetrazolino, formyl, C₂-C₅ alkylcarbonyl, C₂-C₅ haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl or C₁-C₆ hydroxyalkyl;

R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, methylamino and dimethylamino;

R₅ represents hydrogen, C₁-C₁₂-alkylsulfonyl, C₁-C₁₂ alkyl, C₃-C₁₂ alkenyl, C₃-C₁₂ alkynyl, or is C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, azido, formyl, C₂-C₇alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-, (R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—, (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein the group B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—, —ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)2-, —S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—, —C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₅cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, in turn, are mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, mercapto, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is selected from A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- and A-O—(C₃-C₈cycloalkyl)-;

wherein A is a three- to ten-membered monocyclic or fused bicyclic ring system which can be aromatic, partially saturated or fully saturated and can contain 1 to 4 hetero atoms selected from the group consisting of nitrogen, oxygen and sulphur, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the three- to ten-membered ring system to be itself mono- or polysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy, ═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈ halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, C₃-C₈ halocycloalkyloxy, C₃-C₈ cycloalkenyloxy, C₃-C₈ halocycloalkenyloxy, benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy, phenyl and phenoxy, in turn, may be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇ alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₄-C₉ cycloalkoxycarbonyl and benzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted by substituents independently selected from the group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

A4) by substituents independently selected from the group consisting of hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl, ═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄ alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and ═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionally substituted by one or more group selected from the group consisting of halogen, methyl, halomethyl; or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl, C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R₆ is hydrogen;

R₇ is hydrogen or C₁-C₄ alkyl.

In another group of compounds of formula I, R₁ and R₂ are each independently selected from hydrogen or C₁-C₄ alkyl;

or R₁ and R₂ together with the nitrogen atom to which they are attached form a pyrrolidine or piperidine;

R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, formyl, phenyl, C₂-C₄ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl or C₁-C₆ hydroxyalkyl;

R₄ is selected from fluorine, chlorine, bromine, C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, and C₃-C₆ cycloalkyl;

R₅ is selected from G¹, G², G³-G⁴, G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹², G¹³, G¹⁴, G¹⁵ and G¹⁶;

R₆ is hydrogen;

R₇ is selected from hydrogen or C₁-C₄ alkyl;

G¹ is a C₈-C₁₀ fused bicyclic ring system which may be saturated or comprise one carbon-carbon double bond and is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano;

G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

G³ is phenyl, which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionally substituted by one or more halogen;

G⁴ is C₃-C₁₂ cycloalkyl which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionally substituted by one or more halogen;

G⁵ is C₃-C₇ cycloalkyl, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆-alkenyloxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, phenoxy, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

G⁷ is methylene;

G⁸ is

G⁹ is

G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylsulfonyl, phenyl, 2-phenyl-ethynyl and 2-phenyl-ethyl;

G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy;

G¹² is

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄ C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

G¹⁴ is

G¹⁵ is

G¹⁶ is

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 to 4 members selected from the group consisting of N, N(R^(69′)), O and S (for example, pyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazole or tetrazole), it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(1′) is selected from the group consisting of hydrogen, fluorine, C₁-C₄-alkyl, C₁-C₄-haloalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(15′) and R^(16′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

R^(26′) is C(R^(36′))₂, N—OH, N—O—C₁-C₄-alkyl, N—O—C₂-C₄-alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O wherein the N—O-benzyl and N—O-phenyl may be substituted by one or more groups independently selected from the group consisting of halogen, methyl and halomethyl;

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selected from the group consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl and phenyl;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄ alkyl;

R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(50′) is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄ alkylthio;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxy, C₂-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen;

R^(61′) and R^(62′) are selected independently of each other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R⁶⁷ and R^(68′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(69′) is selected from hydrogen, C₁-C₄ alkyl and C₁-C₄ alkylcarboxy;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r, s and t are independently selected from 0 and 1.

In another group of compounds of formula I, R₁ and R₂ are each C₁-C₄ alkyl;

R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄ alkylsulfonyl;

R₄ is selected from methyl, ethyl, methoxy, fluorine and chlorine;

R₆ is hydrogen;

R₇ is hydrogen or C₁-C₄ alkyl.

In another group of compounds, R₁ and R₂ are each independently selected from methyl, ethyl and isopropyl;

R₃ represents hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, cyclopropyl, ethynyl or C₁-C₄ alkoxy;

R₄ is selected from methyl, methoxy, fluorine and chlorine;

R₆ is hydrogen;

R₇ is hydrogen.

In another group of compounds, R₁ is methyl;

R₂ is ethyl;

R₃ is selected from hydrogen, bromine, iodine, methyl, CHF₂, cyclopropyl, ethynyl and methoxy;

R₄ is methyl;

R₆ is hydrogen;

R₇ is hydrogen.

In another group of compounds, G¹ is a C₉-C₁₀ fused bicyclic ring system which may be saturated or comprise one carbon-carbon double bond and is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl;

G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or more groups independently selected from halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

G³ is phenyl, which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ fluoroalkyl, C₁-C₄ alkoxy and halogen;

G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionally substituted by one or more halogen;

G⁵ is C₃-C₇ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy, C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio;

G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, phenyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)2, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy;

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O;

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 to 4 members selected from the group consisting of N, N(R^(69′)), O and S (for example, pyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazole or tetrazole), it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(1′) is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl and C₁-C₄ fluoroalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, cyano, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are independently selected from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃ and CF₂CF₃;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O, or C(R^(36′))₂;

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selected from the group consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄ alkyl;

R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from a group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected from the group consisting of hydrogen, fluorine, chlorine, bromine, iodine, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, difluoromethoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R^(50′)is selected from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄ haloalkoxy;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, cyano, halogen, C₁-C₆ alkyl and C₁-C₆ haloalkyl; provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen;

R^(61′) and R^(62′) are selected independently of each other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selected independently of each other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy;

R^(69′) is selected from hydrogen, C₁-C₄ alkyl and C₁-C₄ alkylcarboxy;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r and s are 0 and t is 1 or 0.

In another group of compounds, G¹ is a saturated C₁₀ fused bicyclic ring system which is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl;

G² is a C₅-C₆ cycloalkenyl group optionally substituted by one or more fluorine atoms;

G³ is phenyl, which is optionally substituted by one or more groups independently selected from C₁-C₄ alkyl, CHF₂, CF₃, C₁-C₄ alkoxy and halogen;

G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or more groups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy and halogen;

G⁵ is C₅-C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂ and C₂-C₆ haloalkyl;

G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, ON, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy.

G⁷ is methylene;

G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from hydrogen, halogen, ON, OH, methyl, ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy, phenyl and OCHF₂;

G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O;

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 to 4 members selected from the group consisting of N, N(R^(69′)), O and S it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzyl are optionally substituted by halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(1′) is selected from the group consisting of hydrogen, fluorine, methyl, CH₂F and CF₃;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, methyl, CH₂F, CF₃ and methoxy;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂, CF₃ and C₁-C₄ alkoxy;

R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are each independently selected from hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the group consisting of hydrogen, methyl, fluorine, chlorine, bromine, ethyl, CH₂F, CHF₂ and CF₃ and isopropyl;

R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O, C₂-C₄ alkenyloxy or C(R^(36′));

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selected from the group consisting of hydrogen, C₁-C₄ alkyl and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which they are attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄ alkyl;

R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are independently selected from the group consisting of hydrogen, fluorine, methyl and trifluoromethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected from the group consisting of hydrogen, fluorine, chlorine, bromine, iodine, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R⁵⁰, R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently of each other, from the group consisting of hydrogen, fluorine, methyl, CH₂F and CF₃;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂ and CF₃;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen;

R^(61′) and R^(62′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, CHF₂ and CF₃;

R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selected independently of each other from the group consisting of hydrogen, fluoro, methyl, ethyl, methoxy, difluoromethoxy, trifluoromethoxy, CHF₂ and CF₃;

R^(69′) is selected from hydrogen and C₁-C₄ alkyl;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r and s are 0 and t is 1 or 0.

In another group of compounds, G¹ is a saturated C₁₀ fused bicyclic ring system;

G² is a C₅-C₆ cycloalkenyl group;

G³ is phenyl;

G⁴ is cyclohexyl or cyclopentyl;

G⁵ is C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂ and —CH(CH₃)—CH(CH₃)₂;

G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more methyl, bromine, iodine or chlorine;

G⁷ is methylene;

G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, ethenyl, methoxy, ethoxy, iso-propyloxy, phenyl, CHF₂, CF₃, CHF—CH₃ and OCHF₂;

G¹¹ is methylene substituted by at least one group independently selected from methyl, CF₃ and ethyl;

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which is optionally substituted by one or more groups independently selected from halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy and =0;

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring system which can contain 1 or 2 members selected from the group consisting of N, O and S, it not being possible for each ring system to contain —O—O—, —S—S— and —O—S— fragments, and it being possible for the five- to six-membered ring system to be itself mono- or polysubstituted by groups selected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl;

R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ alkoxy;

R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′), R^(22′), R^(23′), R^(24′) and R^(25′) are each independently selected from hydrogen, methyl, ethyl and isopropyl;

R^(23′), R^(24′) and R^(25′) are each independently selected from hydrogen, fluorine, chlorine, bromine, methyl, ethyl and isopropyl;

R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O, C₂-C₄ alkenyloxy and C(R^(36′));

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) are each hydrogen or methyl;

or R^(27′) and R^(28′) together with the two carbon atoms to which they are attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄ alkyl;

R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected from the group consisting of hydrogen, fluorine, chlorine, methyl, CF₃, CHF₂, CH₂F, methoxy, difluoromethoxy and trifluoromethoxy;

R^(50′), R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are each hydrogen;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently of each other, from the group consisting of hydrogen and halogen;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen;

R^(61′), R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are hydrogen;

R^(69′) is hydrogen;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r, s and t are each 0.

In another preferred group of compounds, R⁵ is G¹.

In another preferred group of compounds, R⁵ is G².

In another preferred group of compounds, R⁵ is G³-G⁴.

In another preferred group of compounds, R⁵ is G⁵.

In another preferred group of compounds, R⁵ is G⁶-G⁷.

In another preferred group of compounds, R⁵ is G⁸.

In another preferred group of compounds, R⁵ is G⁹.

In another preferred group of compounds, R⁵ is G¹⁰-G¹¹.

In another preferred group of compounds, R⁵ is G¹².

In another preferred group of compounds, R⁵ is G¹³.

In another preferred group of compounds, R⁵ is G¹⁴.

In another preferred group of compounds, R⁵ is G¹⁵.

In another preferred group of compounds, R⁵ is G¹⁶.

In a further group of compounds, R₁ is selected from R^(1a) and R^(1b);

R₂ is methyl;

R₃ is selected from R^(3a), R^(3b), R^(3c), R^(3d), R^(3e), R^(3f), R^(3g), R^(3h), R^(3i), R^(3j), R^(3k), R^(3l), R^(3m), R^(3n), R^(3o), R^(3p), R^(3q), R^(3r), R^(3s), R^(3t);

R⁴ is selected from R_(4a), R_(4b), R_(4c), R^(4d), R^(4e), R_(4f);

R₅ is selected from R^(5a), R^(5b), R^(5c), R^(5d), R^(5e), R^(5f), R^(5g), R^(5h), R^(5j), R^(5k), R^(5l), R^(5m), R^(5n), R^(5o), R^(5p), R^(5q), R^(5r), R^(5s), R^(5t), R^(5u), R^(5v), R^(5x), R^(5y), R^(5z), R^(5ab), R^(5ac), R^(5ad), R^(5ae), R^(5af), R^(5ag), R^(5ah), R^(5aj), R^(5ak), R^(5al), R^(5am), R^(5aa), R^(5bb), R^(5cc), R^(5dd), R^(5ee), R^(5ff), R^(5gg), R^(5hh), R^(5jj), R^(5kk), R^(5ll), R^(5mm), R^(5nn), R^(5oo), R^(5pp), R^(5qq), R^(5rr), R^(5ss), R^(5tt), R^(5uu), R^(5vv), R^(5ww), R^(5xx), R^(5zz), R^(5ba), R^(5bc), R^(5bd), R^(5be), R^(5bf), R^(5bg), R^(5bh), R^(5bi), R^(5bj), R^(5bk), R^(5bl), R^(5bm), R^(5bn), R^(5bo), R^(5bp), R^(5bq), R^(5br), R^(5bs), R^(5bt), R^(5bu), R^(5bv), R^(5bw), R^(5bx), R^(5by), R^(5bz), R^(5ca), R^(5cb), R^(5cd), R^(5ce), R^(5cf), R^(5cg), R^(5ch), R^(5ci), R^(5cj), R^(5ck), R^(5cl), R^(5cm), R^(5cn), R^(5o), R^(5cq), R^(5cr), R^(5cs), R^(5ct), R^(5cu), R^(5cv), R^(5cw), R^(5cx), R^(5cy), R^(5cz), R^(5da), R^(5db), R^(5dc), R^(5de), R^(5df), R^(5dg), R^(5dh), R^(5di), R^(5dj), R^(5dk), R^(5dl), R^(5dm), R^(5dn), R^(5do), R^(5dp), R^(5dq), R^(5dr), R^(5ds), R^(5dt), R^(5du), R^(5dv), R^(5dw), R^(5dx), R^(5ea), R^(5eb), R^(5ec), R^(5ed), R^(5ef), R^(5eg), R^(5eh), R^(5ei), R^(5ej), R^(5ek), R^(5el), R^(5em), R^(5en), R^(5eo), R^(5ep), R^(5eq), R^(5er), R^(5es), R^(5et), R^(5eu), R^(5ev), R^(5ex), R^(5ey), R^(5ez), R^(5fa), R^(5fb), R^(5fc), R^(5fd), R^(5fe), R^(5fg), R^(5fh), R^(5fi), R^(5fj), R^(5fk), R^(5fl), R^(5fm), R^(5fn), R^(5fo), R^(5fp), R^(5fq), R^(5fr), R^(5fs), R^(5ft), R^(5fu), R^(5fv), R^(5fw);

R₆ is selected from R^(6a), R^(6b) and R^(6c);

R₇ is H;

R^(1a) is selected from ethyl and isopropyl;

R^(1b) is ethyl;

R^(3a) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, CCH, CH═CH₂, H₂C═C—(CH₃), cyclopropyl, halomethyl, haloethyl, methoxy, halomethoxy, ethoxy, haloethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO, CH₂OH, CH(OH)Me and CO-Me;

R^(3b) is selected from hydrogen, F, Cl, Br, I, cyano, methyl, ethyl, isopropyl, fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF, methoxy and ethoxy;

R^(3c) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl, fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF, methoxy and ethoxy;

R^(3d) is selected from hydrogen, halogen, cyano, methyl, ethyl, isopropyl, C≡CH, CH═CH₂, H₂C═C—(CH₃), cyclopropyl, halomethyl, haloethyl, methoxy, ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO and CO-Me;

R^(3b) is selected from hydrogen, F, Cl, Br, I, cyano, methyl, ethyl, isopropyl, fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF, methoxy and ethoxy;

R^(3c) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl, fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF, methoxy and ethoxy;

R^(3e) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, C═CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO, CH₂OH, CH(OH)Me and CO-Me;

R^(3f) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, C═CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R^(3g) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R^(3h) is selected from hydrogen, Br, I, methyl, ethyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F and methoxy;

R^(3i) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO and CO-Me;

R^(3′) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, halomethyl, haloethyl, methoxy and ethoxy;

R^(3k) is selected from hydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, methoxy and ethoxy;

R^(3l) is selected from hydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, methoxy and ethoxy;

R^(3m) is selected from hydrogen, F, Br, I, methyl, ethyl, CHF₂ and methoxy;

R^(3n) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO, CH₂OH, CH(OH)Me and CO-Me;

R³⁰ is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl and halomethylsulfonyl;

R^(3p) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy and ethoxy;

R^(3q) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R^(3r) is selected from hydrogen, Br, I, methyl, cyclopropyl, C≡CH, CH═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃ and methoxy;

R^(3s) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, tert-butyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, halomethoxy, ethoxy, haloethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO and C(═O)Me;

R^(3t) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl, cyclopropyl, tert-butyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy, halomethoxy, ethoxy, haloethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO and C(═O)Me;

R_(4a) is selected from F, Cl, Br, C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl and C₁-C₄ cycloalkyl;

R_(4b) is selected from F, Cl, methyl, ethyl, ethenyl, propyl, propenyl, isopropyl, isopropenyl, cyclopropanyl, methoxy, ethoxy, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoromethyl

R_(4c) is selected from methyl, ethyl, methoxy, F and Cl;

R_(4d) is selected from methyl, methoxy, F and Cl;

R_(4e) is selected from methyl;

R_(4f) is selected from methoxy, F and Cl;

R^(5a) is a 3- to 6-membered cycloalkenyl group, or a 3- to 6-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5b) is a 3- to 6-membered cycloalkenyl group, or a 3- to 6-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5c) is a 3- to 6-membered cycloalkenyl group, or a 3- to 6-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5d) is a 5-membered cycloalkenyl group, or a 5-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5e) is a 5-membered cycloalkenyl group, or a 5-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5f) is a 5-membered cycloalkenyl group, or a 5-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R⁵⁹ is a 6-membered cycloalkenyl group, or a 6-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄ C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5h) is a 6-membered cycloalkenyl group, or a 6-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5j) is a 6-membered cycloalkenyl group, or a 6-membered cycloalkenyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5k) is a 3- to 7-membered cycloalkyl group, or a 3- to 7-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5l) is a 3- to 7-membered cycloalkyl group, or a 3- to 7-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5m) is a 3- to 7-membered cycloalkyl group, or a 3- to 7-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5n) is a 3-membered cycloalkyl group, or a 3-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄ C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5o) is a 3-membered cycloalkyl group, or a 3-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5p) is a 3-membered cycloalkyl group, or a 3-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5q) is a 4-membered cycloalkyl group, or a 4-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄ C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5r) is a 4-membered cycloalkyl group, or a 4-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5s) is a 4-membered cycloalkyl group, or a 4-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5t) is a 5-membered cycloalkyl group, or a 5-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄ C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5u) is a 5-membered cycloalkyl group, or a 5-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5v) is a 5-membered cycloalkyl group, or a 5-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5x) is a 6-membered cycloalkyl group, or a 6-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5y) is a 6-membered cycloalkyl group, or a 6-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5z) is a 6-membered cycloalkyl group, or a 6-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5ab) is a 7-membered cycloalkyl group, or a 7-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5ac) is a 7-membered cycloalkyl group, or a 7-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5ad) is a 7-membered cycloalkyl group, or a 7-membered cycloalkyl group that can be mono- to polysubstituted by substituents independently selected from the group consisting of halogen, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5ae) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each independently selected from hydrogen, fluoro, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5af) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each independently selected from hydrogen, fluoro, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5ag) is G⁸ wherein R¹, R², R^(3′), R^(4′) and R^(5′) are each independently selected from hydrogen, fluoro, methyl, ethyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, methoxy, ethoxy, S—CH₃ and S—CH₂CH₃;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(5ah) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each independently selected from hydrogen, fluoro, methyl, CHF₂, CF₃ and methoxy;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁—C alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5aj) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each independently selected from hydrogen, fluoro, methyl, CHF₂, CF₃ and methoxy;

and wherein R^(11′), R¹², R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5ak) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each independently selected from hydrogen, fluoro, methyl, CHF₂, CF₃ and methoxy;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(5al) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5am) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen;

and wherein R^(11′), R¹², R¹³ and R^(14′) are each independently selected from hydrogen, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5aa) is G⁸ wherein R¹, R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen;

and wherein R^(11′), R¹², R^(13′) and R^(14′) are each independently selected from hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(5bb) is a benzyl group, wherein the phenyl ring is substituted by at least one fluorine and optionally by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5cc) is a benzyl group, wherein the phenyl ring is substituted by at least one fluorine and optionally by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

R^(5dd) is a benzyl group, wherein the phenyl ring is substituted by at least one fluorine and optionally by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy and C₁-C₆ alkylthio;

R^(5ee) is a benzyl group, wherein the phenyl ring is substituted by at least one fluorine and optionally by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₃-C₆ cycloalkyl and C₁-C₄ alkoxy;

R^(5ff) is a benzyl group, wherein the methylene portion is substituted by at least one group independently selected from the group consisting of hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5gg) is a benzyl group, wherein the methylene portion is substituted by at least one group independently selected from the group consisting of hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5hh) is a benzyl group, wherein the methylene portion is substituted one group independently selected from the group consisting of C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl

R^(5jj) is a benzyl group, wherein the methylene portion is substituted by one group independently selected from the group consisting of hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5kk) is a benzyl group, wherein the methylene portion is substituted one group independently selected from the group consisting of methyl, ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5ll) is a benzyl group, wherein the methylene portion is substituted by one group independently selected from the group consisting of methyl, ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5mm) is a benzyl group, wherein the methylene portion is substituted by at least one group independently selected from the group consisting of hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, OH, SH, CHO C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

R^(5nn) is a benzyl group, wherein the methylene portion is substituted one group independently selected from the group consisting of C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, OH, SH, CHO C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

R^(5oo) is a benzyl group, wherein the methylene portion is substituted one group independently selected from the group consisting of methyl, ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, OH, SH, CHO C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

R^(5pp) is a benzyl group, wherein the methylene portion is substituted by at least one group independently selected from the group consisting of hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CC₂, C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

R^(5qq) is a benzyl group, wherein the methylene portion is substituted one group independently selected from the group consisting of C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

R^(5rr) is a benzyl group, wherein the methylene portion is substituted one group independently selected from the group consisting of methyl, ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or more groups independently selected from the group consisting of hydrogen, halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

R^(5ss) is G⁹ wherein R^(15′) and R¹⁶ are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

R^(5tt) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5uu) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5vv) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5vv) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5xx) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5zz) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, fluoromethyl and fluoroethyl;

R^(5ba) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is either 0 or 1;

R^(5bc) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is either 0 or 1;

R^(5bd) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(22′) to R^(24′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is either 0 or 1;

R^(5be) is G⁹ wherein R^(15′) and R¹⁶ are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is either 0 or 1;

R^(5bf) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is either 0 or 1;

R^(5bg) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(5bh) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is either 0 or 1;

R^(5bi) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is either 0 or 1;

R^(5bj) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is either 0 or 1;

R^(5bk) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is either 0 or 1;

R^(5bl) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is hydrogen;

R^(22′) to R^(24′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is either 0 or 1;

R^(5bm) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 0;

R^(5bn) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 0;

R^(5bo) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 0;

R^(5bp) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 0;

R^(5bq) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 0;

R^(5br) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R¹⁶, R¹⁷, R^(18′), R¹⁹, R^(20′), R^(21′) and R²² is selected independently of each other, from the group consisting of hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 0;

R^(5bs) is G⁹ wherein R^(15′) and R¹⁶ are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 0;

R^(5bt) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 0;

R^(5bu) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 0;

R^(5bv) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 0;

R^(5bw) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 0;

R^(5bx) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 0;

R^(5by) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 0;

R^(5bz) is G⁹ wherein each R^(15′), R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R²¹ and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 0;

R^(5ca) is G⁹ wherein each R^(15′), R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 0;

R^(5cb) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 0;

R^(5cd) is G⁹ wherein R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 0;

R^(5ce) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 0;

R^(5cf) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 1;

R^(5cg) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R²¹ and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 1;

R^(5ch) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 1;

R^(5ci) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 1;

R^(5cj) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 1;

R^(5ck) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl; each R^(16′), R¹⁷, R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is selected independently of each other, from the group consisting of hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio;

n is 1;

R^(5cl) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R²² are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 1;

R^(5cm) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 1;

R^(5cn) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 1;

R^(5co) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 1;

R^(5cp) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 1;

R^(5cq) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

n is 1;

R^(5cr) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 1;

R^(5cs) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 1;

R^(5ct) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R²¹ and R²² are selected independently of each other, from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 1;

R^(5cu) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 1;

R^(5cv) is G⁹ wherein R^(15′) and R^(16′) are selected independently of each other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) are selected independently of each other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 1;

R^(5cw) is G⁹ wherein R^(15′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) is hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other, from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is 1;

R^(5cx) is G¹⁴ wherein G¹⁴ is

wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5cy) is G¹⁴ wherein R³⁷, R³⁸, R³⁹, R⁴⁰, R⁴¹, R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5cz) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5da) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5db) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dc) is G¹⁴ wherein R^(37′) is selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5de) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′), and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5df) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoromethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dg) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dh) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5di) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dj) is G¹⁴ wherein R^(37′) is selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dk) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dl) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dm) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dn) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5do) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy; p and q are independently selected from 0 and 1;

R^(5dp) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R⁴⁰, R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dq) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, and C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dr) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5ds) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dt) is G¹⁴ wherein R^(37′), R^(38′), R³⁹, R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5du) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dv) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dw) is G¹⁴ wherein R^(37′) and R^(37′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5dx) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ea) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5eb) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently from each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ec) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ed) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ef) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5eg) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5eh) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5ei) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5ej) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R⁴⁰, R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5ek) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5el) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5em) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5en) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R⁴⁰, R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5eo) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R⁴², R^(43′) and R^(44′) are independently selected of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5ep) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R⁴¹, R⁴², R^(43′) and R^(44′) are each hydrogen;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5eq) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5er) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5es) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5et) is G¹⁴ wherein R^(37′), R^(38′), R³⁹, R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5eu) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5ev) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5ex) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5ey) is G¹⁴ wherein R³⁷ and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5ez) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoromethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fa) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fb) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fc) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fd) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen; R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fe) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fg) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fh) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fi) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fj) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fk) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fl) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fm) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fn) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fo) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fp) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fq) is G¹⁴ wherein R^(37′) is selected from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fr) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently of each other from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fs) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R⁴⁰, R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5ft) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fu) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44″) are selected independently of each other from the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fv) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fw) is G¹⁴ wherein R^(37′) is selected from hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of each other from the group consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R⁴⁶, R^(47′), R^(48′) and R^(49′) are selected, independently of each other, from the group consisting of hydrogen, F, Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(6a) is selected from hydrogen and SH;

R^(6b) is hydrogen;

R^(6c) is SH.

Each line of Table N describes a preferred sub-group from N1-N757 of this group. For reasons of clarity, note that in these sub-groups, R₂ is always methyl and R₇ is always hydrogen. For example, sub-group N1 is a group of compounds of formula (I) wherein

R₁ is R^(1b);

R₂ is methyl;

R₃ is R^(3a);

R₄ is R^(4c);

R₅ is R^(5a);

R₆ is R^(6b);

R₇ is H.

TABLE N R₁ R₃ R₄ R₅ R₆ N1 R^(1b) R^(3a) R^(4c) R^(5a) R^(6b) N2 R^(1b) R^(3b) R^(4d) R^(5a) R^(6b) N3 R^(1b) R^(3c) R^(4e) R^(5a) R^(6b) N4 R^(1b) R^(3a) R^(4c) R^(5b) R^(6b) N5 R^(1b) R^(3b) R^(4d) R^(5b) R^(6b) N6 R^(1b) R^(3c) R^(4e) R^(5b) R^(6b) N7 R^(1b) R^(3a) R^(4c) R^(5c) R^(6b) N8 R^(1b) R^(3b) R^(4d) R^(5c) R^(6b) N9 R^(1b) R^(3c) R^(4e) R^(5c) R^(6b) N10 R^(1b) R^(3a) R^(4c) R^(5d) R^(6b) N11 R^(1b) R^(3b) R^(4d) R^(5d) R^(6b) N12 R^(1b) R^(3c) R^(4e) R^(5d) R^(6b) N13 R^(1b) R^(3a) R^(4c) R^(5e) R^(6b) N14 R^(1b) R^(3b) R^(4d) R^(5e) R^(6b) N15 R^(1b) R^(3c) R^(4e) R^(5e) R^(6b) N16 R^(1b) R^(3a) R^(4c) R^(5f) R^(6b) N17 R^(1b) R^(3b) R^(4d) R^(5f) R^(6b) N18 R^(1b) R^(3c) R^(4e) R^(5f) R^(6b) N19 R^(1b) R^(3a) R^(4c) R^(5g) R^(6b) N20 R^(1b) R^(3b) R^(4d) R^(5g) R^(6b) N21 R^(1b) R^(3c) R^(4e) R^(5g) R^(6b) N22 R^(1b) R^(3a) R^(4c) R^(5h) R^(6b) N23 R^(1b) R^(3b) R^(4d) R^(5h) R^(6b) N24 R^(1b) R^(3c) R^(4e) R^(5h) R^(6b) N25 R^(1b) R^(3a) R^(4c) R^(5j) R^(6b) N26 R^(1b) R^(3b) R^(4d) R^(5j) R^(6b) N27 R^(1b) R^(3c) R^(4e) R^(5j) R^(6b) N28 R^(1b) R^(3d) R^(4c) R^(5k) R^(6b) N29 R^(1b) R^(3b) R^(4d) R^(5k) R^(6b) N30 R^(1b) R^(3c) R^(4e) R^(5k) R^(6b) N31 R^(1b) R^(3d) R^(4c) R^(5l) R^(6b) N32 R^(1b) R^(3b) R^(4d) R^(5l) R^(6b) N33 R^(1b) R^(3c) R^(4e) R^(5l) R^(6b) N34 R^(1b) R^(3d) R^(4c) R^(5m) R^(6b) N35 R^(1b) R^(3b) R^(4d) R^(5m) R^(6b) N36 R^(1b) R^(3c) R^(4e) R^(5m) R^(6b) N37 R^(1b) R^(3d) R^(4c) R^(5n) R^(6b) N38 R^(1b) R^(3b) R^(4d) R^(5n) R^(6b) N39 R^(1b) R^(3c) R^(4e) R^(5n) R^(6b) N40 R^(1b) R^(3d) R^(4c) R^(5o) R^(6b) N41 R^(1b) R^(3b) R^(4d) R^(5o) R^(6b) N42 R^(1b) R^(3c) R^(4e) R^(5o) R^(6b) N43 R^(1b) R^(3d) R^(4c) R^(5p) R^(6b) N44 R^(1b) R^(3b) R^(4d) R^(5p) R^(6b) N45 R^(1b) R^(3c) R^(4e) R^(5p) R^(6b) N46 R^(1b) R^(3d) R^(4c) R^(5q) R^(6b) N47 R^(1b) R^(3b) R^(4d) R^(5q) R^(6b) N48 R^(1b) R^(3c) F^(4e) R^(5q) R^(6b) N49 R^(1b) R^(3d) R^(4c) R^(5r) R^(6b) N50 R^(1b) R^(3b) R^(4d) R^(5r) R^(6b) N51 R^(1b) R^(3c) R^(4e) R^(5r) R^(6b) N52 R^(1b) R^(3d) R^(4c) R^(5s) R^(6b) N53 R^(1b) R^(3b) R^(4d) R^(5s) R^(6b) N54 R^(1b) R^(3c) R^(4e) R^(5s) R^(6b) N55 R^(1b) R^(3d) R^(4c) R^(5t) R^(6b) N56 R^(1b) R^(3b) R^(4d) R^(5t) R^(6b) N57 R^(1b) R^(3c) R^(4e) R^(5t) R^(6b) N58 R^(1b) R^(3d) R^(4c) R^(5u) R^(6b) N59 R^(1b) R^(3b) R^(4d) R^(5u) R^(6b) N60 R^(1b) R^(3c) R^(4e) R^(5u) R^(6b) N61 R^(1b) R^(3d) R^(4c) R^(5v) R^(6b) N62 R^(1b) R^(3b) R^(4d) R^(5v) R^(6b) N63 R^(1b) R^(3c) R^(4e) R^(5v) R^(6b) N64 R^(1b) R^(3d) R^(4c) R^(5x) R^(6b) N65 R^(1b) R^(3b) R^(4d) R^(5x) R^(6b) N66 R^(1b) R^(3c) R^(4e) R^(5x) R^(6b) N67 R^(1b) R^(3d) R^(4c) R^(5y) R^(6b) N68 R^(1b) R^(3b) R^(4d) R^(5y) R^(6b) N69 R^(1b) R^(3c) R^(4e) R^(5y) R^(6b) N70 R^(1b) R^(3d) R^(4c) R^(5z) R^(6b) N71 R^(1b) R^(3b) R^(4d) R^(5z) R^(6b) N72 R^(1b) R^(3c) R^(4e) R^(5z) R^(6b) N73 R^(1b) R^(3d) R^(4c) R^(5ab) R^(6b) N74 R^(1b) R^(3b) R^(4d) R^(5ab) R^(6b) N75 R^(1b) R^(3c) R^(4e) R^(5ab) R^(6b) N76 R^(1b) R^(3d) R^(4c) R^(5ac) R^(6b) N77 R^(1b) R^(3b) R^(4d) R^(5ac) R^(6b) N78 R^(1b) R^(3c) R^(4e) R^(5ac) R^(6b) N79 R^(1b) R^(3d) R^(4c) R^(5ad) R^(6b) N80 R^(1b) R^(3b) R^(4d) R^(5ad) R^(6b) N81 R^(1b) R^(3c) R^(4e) R^(5ad) R^(6b) N82 R^(1b) R^(3e) R^(4c) R^(5bb) R^(6b) N83 R^(1b) R^(3f) R^(4c) R^(5bb) R^(6b) N84 R^(1b) R^(3g) R^(4e) R^(5bb) R^(6b) N85 R^(1b) R^(3h) R^(4e) R^(5bb) R^(6b) N86 R^(1b) R^(3e) R^(4c) R^(5cc) R^(6b) N87 R^(1b) R^(3f) R^(4c) R^(5cc) R^(6b) N88 R^(1b) R^(3g) R^(4e) R^(5cc) R^(6b) N89 R^(1b) R^(3h) R^(4e) R^(5cc) R^(6b) N90 R^(1b) R^(3e) R^(4c) R^(5dd) R^(6b) N91 R^(1b) R^(3f) R^(4c) R^(5dd) R^(6b) N92 R^(1b) R^(3g) R^(4e) R^(5dd) R^(6b) N93 R^(1b) R^(3h) R^(4e) R^(5dd) R^(6b) N94 R^(1b) R^(3e) R^(4c) R^(5ee) R^(6b) N95 R^(1b) R^(3f) R^(4c) R^(5ee) R^(6b) N96 R^(1b) R^(3g) R^(4e) R^(5ee) R^(6b) N97 R^(1b) R^(3h) R^(4e) R^(5ee) R^(6b) N98 R^(1b) R^(3i) R^(4c) R^(5ae) R^(6a) N99 R^(1b) R^(3j) R^(4c) R^(5af) R^(6b) N100 R^(1b) R^(3k) R^(4c) R^(5ag) R^(6a) N101 R^(1b) R^(3k) R^(4c) R^(5ag) R^(6b) N102 R^(1b) R^(3l) R^(4c) R^(5ag) R^(6c) N103 R^(1b) R^(3i) R^(4e) R^(5ae) R^(6a) N104 R^(1b) R^(3j) R^(4e) R^(5af) R^(6b) N105 R^(1b) R^(3k) R^(4e) R^(5ag) R^(6a) N106 R^(1b) R^(3k) R^(4e) R^(5ag) R^(6b) N107 R^(1b) R^(3l) R^(4e) R^(5ag) R^(6c) N108 R^(1b) R^(3i) R^(4f) R^(5ae) R^(6a) N109 R^(1b) R^(3j) R^(4f) R^(5af) R^(6b) N110 R^(1b) R^(3k) R^(4f) R^(5ag) R^(6a) N111 R^(1b) R^(3k) R^(4f) R^(5ag) R^(6b) N112 R^(1b) R^(3l) R^(4f) R^(5ag) R^(6c) N113 R^(1b) R^(3m) R^(4c) R^(5ae) R^(6a) N114 R^(1b) R^(3m) R^(4c) R^(5af) R^(6b) N115 R^(1b) R^(3m) R^(4c) R^(5ag) R^(6a) N116 R^(1b) R^(3m) R^(4c) R^(5ag) R^(6b) N117 R^(1b) R^(3m) R^(4c) R^(5ag) R^(6c) N118 R^(1b) R^(3m) R^(4e) R^(5ae) R^(6a) N119 R^(1b) R^(3m) R^(4e) R^(5af) R^(6b) N120 R^(1b) R^(3m) R^(4e) R^(5ag) R^(6a) N121 R^(1b) R^(3m) R^(4e) R^(5ag) R^(6b) N122 R^(1b) R^(3m) R^(4e) R^(5ag) R^(6c) N123 R^(1b) R^(3m) R^(4f) R^(5ae) R^(6a) N124 R^(1b) R^(3m) R^(4f) R^(5af) R^(6b) N125 R^(1b) R^(3m) R^(4f) R^(5ag) R^(6a) N126 R^(1b) R^(3m) R^(4f) R^(5ag) R^(6b) N127 R^(1b) R^(3m) R^(4f) R^(5ag) R^(6c) N128 R^(1b) R^(3i) R^(4c) R^(5ah) R^(6a) N129 R^(1b) R^(3j) R^(4c) R^(5ai) R^(6b) N130 R^(1b) R^(3k) R^(4c) R^(5ak) R^(6a) N131 R^(1b) R^(3k) R^(4c) R^(5ak) R^(6b) N132 R^(1b) R^(3l) R^(4c) R^(5ak) R^(6c) N133 R^(1b) R^(3i) R^(4e) R^(5ah) R^(6a) N134 R^(1b) R^(3j) R^(4e) R^(5ai) R^(6b) N135 R^(1b) R^(3k) R^(4e) R^(5ak) R^(6a) N136 R^(1b) R^(3k) R^(4e) R^(5ak) R^(6b) N137 R^(1b) R^(3l) R^(4e) R^(5ak) R^(6c) N138 R^(1b) R^(3i) R^(4f) R^(5ah) R^(6a) N139 R^(1b) R^(3j) R^(4f) R^(5ai) R^(6b) N140 R^(1b) R^(3k) R^(4f) R^(5ak) R^(6a) N141 R^(1b) R^(3k) R^(4f) R^(5ak) R^(6b) N142 R^(1b) R^(3l) R^(4f) R^(5ak) R^(6c) N143 R^(1b) R^(3m) R^(4c) R^(5ah) R^(6a) N144 R^(1b) R^(3m) R^(4c) R^(5ai) R^(6b) N145 R^(1b) R^(3m) R^(4c) R^(5ak) R^(6a) N146 R^(1b) R^(3m) R^(4c) R^(5ak) R^(6b) N147 R^(1b) R^(3m) R^(4c) R^(5ak) R^(6c) N148 R^(1b) R^(3m) R^(4e) R^(5ah) R^(6a) N149 R^(1b) R^(3m) R^(4e) R^(5ai) R^(6b) N150 R^(1b) R^(3m) R^(4e) R^(5ak) R^(6a) N151 R^(1b) R^(3m) R^(4e) R^(5ak) R^(6b) N152 R^(1b) R^(3m) R^(4e) R^(5ak) R^(6c) N153 R^(1b) R^(3m) R^(4f) R^(5ah) R^(6a) N154 R^(1b) R^(3m) R^(4f) R^(5ai) R^(6b) N155 R^(1b) R^(3m) R^(4f) R^(5ak) R^(6a) N156 R^(1b) R^(3m) R^(4f) R^(5ak) R^(6b) N157 R^(1b) R^(3m) R^(4f) R^(5ak) R^(6c) N158 R^(1b) R^(3i) R^(4c) R^(5al) R^(6a) N159 R^(1b) R^(3j) R^(4c) R^(5am) R^(6b) N160 R^(1b) R^(3k) R^(4c) R^(5an) R^(6a) N161 R^(1b) R^(3k) R^(4c) R^(5an) R^(6b) N162 R^(1b) R^(3l) R^(4c) R^(5an) R^(6c) N163 R^(1b) R^(3i) R^(4e) R^(5al) R^(6a) N164 R^(1b) R^(3j) R^(4e) R^(5am) R^(6b) N165 R^(1b) R^(3k) R^(4e) R^(5an) R^(6a) N166 R^(1b) R^(3k) R^(4e) R^(5an) R^(6b) N167 R^(1b) R^(3l) R^(4e) R^(5an) R^(6c) N168 R^(1b) R^(3i) R^(4f) R^(5al) R^(6a) N169 R^(1b) R^(3j) R^(4f) R^(5am) R^(6b) N170 R^(1b) R^(3k) R^(4f) R^(5an) R^(6a) N171 R^(1b) R^(3k) R^(4f) R^(5an) R^(6b) N172 R^(1b) R^(3l) R^(4f) R^(5an) R^(6c) N173 R^(1a) R^(3n) R^(4c) R^(5ff) R^(6a) N174 R^(1b) R^(3o) R^(4c) R^(5gg) R^(6b) N175 R^(1b) R^(3o) R^(4c) R^(5gg) R^(6c) N176 R^(1b) R^(3p) R^(4e) R^(5ff) R^(6b) N177 R^(1b) R^(3p) R^(4e) R^(5gg) R^(6b) N178 R^(1b) R^(3q) R^(4e) R^(5ff) R^(6b) N179 R^(1b) R^(3q) R^(4e) R^(5gg) R^(6b) N180 R^(1b) R^(3r) R^(4e) R^(5ff) R^(6b) N181 R^(1b) R^(3r) R^(4e) R^(5gg) R^(6b) N182 R^(1a) R^(3n) R^(4c) R^(5hh) R^(6a) N183 R^(1b) R^(3o) R^(4c) R^(5jj) R^(6b) N184 R^(1b) R^(3o) R^(4c) R^(5jj) R^(6c) N185 R^(1b) R^(3p) R^(4e) R^(5hh) R^(6b) N186 R^(1b) R^(3p) R^(4e) R^(5jj) R^(6b) N187 R^(1b) R^(3q) R^(4e) R^(5hh) R^(6b) N188 R^(1b) R^(3q) R^(4e) R^(5jj) R^(6b) N189 R^(1b) R^(3r) R^(4e) R^(5hh) R^(6b) N190 R^(1b) R^(3r) R^(4e) R^(5jj) R^(6b) N191 R^(1a) R^(3n) R^(4c) R^(5kk) R^(6a) N192 R^(1b) R^(3o) R^(4c) R^(5ll) R^(6b) N193 R^(1b) R^(3o) R^(4c) R^(5ll) R^(6c) N194 R^(1b) R^(3p) R^(4e) R^(5kk) R^(6b) N195 R^(1b) R^(3p) R^(4e) R^(5ll) R^(6b) N196 R^(1b) R^(3q) R^(4e) R^(5kk) R^(6b) N197 R^(1b) R^(3q) R^(4e) R^(5ll) R^(6b) N198 R^(1b) R^(3r) R^(4e) R^(5kk) R^(6b) N199 R^(1b) R^(3r) R^(4e) R^(5ll) R^(6b) N200 R^(1a) R^(3n) R^(4c) R^(5mm) R^(6a) N201 R^(1b) R^(3o) R^(4c) R^(5nn) R^(6b) N202 R^(1b) R^(3o) R^(4c) R^(5nn) R^(6c) N203 R^(1b) R^(3p) R^(4e) R^(5mm) R^(6b) N204 R^(1b) R^(3p) R^(4e) R^(5nn) R^(6b) N205 R^(1b) R^(3q) R^(4e) R^(5mm) R^(6b) N206 R^(1b) R^(3q) R^(4e) R^(5nn) R^(6b) N207 R^(1b) R^(3r) R^(4e) R^(5mm) R^(6b) N208 R^(1b) R^(3r) R^(4e) R^(5nn) R^(6b) N209 R^(1a) R^(3n) R^(4c) R^(5nn) R^(6a) N210 R^(1b) R^(3o) R^(4c) R^(5nn) R^(6b) N211 R^(1b) R^(3o) R^(4c) R^(5nn) R^(6c) N212 R^(1b) R^(3p) R^(4e) R^(5nn) R^(6b) N213 R^(1b) R^(3p) R^(4e) R^(5nn) R^(6b) N214 R^(1b) R^(3q) R^(4e) R^(5nn) R^(6b) N215 R^(1b) R^(3q) R^(4e) R^(5nn) R^(6b) N216 R^(1b) R^(3r) R^(4e) R^(5nn) R^(6b) N217 R^(1b) R^(3r) R^(4e) R^(5nn) R^(6b) N218 R^(1a) R^(3n) R^(4c) R^(5oo) R^(6a) N219 R^(1b) R^(3o) R^(4c) R^(5oo) R^(6b) N220 R^(1b) R^(3o) R^(4c) R^(5oo) R^(6c) N221 R^(1b) R^(3p) R^(4e) R^(5oo) R^(6b) N222 R^(1b) R^(3p) R^(4e) R^(5oo) R^(6b) N223 R^(1b) R^(3q) R^(4e) R^(5oo) R^(6b) N224 R^(1b) R^(3q) R^(4e) R^(5oo) R^(6b) N225 R^(1b) R^(3r) R^(4e) R^(5oo) R^(6b) N226 R^(1b) R^(3r) R^(4e) R^(5oo) R^(6b) N227 R^(1a) R^(3n) R^(4c) R^(5pp) R^(6a) N228 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6b) N229 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6c) N230 R^(1b) R^(3p) R^(4e) R^(5qq) R^(6b) N231 R^(1b) R^(3p) R^(4e) R^(5qq) R^(6b) N232 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b) N233 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b) N234 R^(1b) R^(3r) R^(4e) R^(5qq) R^(6b) N235 R^(1b) R^(3r) R^(4e) R^(5qq) R^(6b) N236 R^(1a) R^(3n) R^(4c) R^(5pp) R^(6a) N237 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6b) N238 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6c) N239 R^(1b) R^(3p) R^(4e) R^(5qq) R^(6b) N240 R^(1b) R^(3p) R^(4e) R^(5qq) R^(6b) N241 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b) N242 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b) N243 R^(1b) R^(3r) R^(4e) R^(5qq) R^(6b) N244 R^(1b) R^(3r) R^(4e) R^(5qq) R^(6b) N245 R^(1a) R^(3n) R^(4c) R^(5rr) R^(6a) N246 R^(1b) R^(3o) R^(4c) R^(5rr) R^(6b) N247 R^(1b) R^(3o) R^(4c) R^(5rr) R^(6c) N248 R^(1b) R^(3p) R^(4e) R^(5rr) R^(6b) N249 R^(1b) R^(3p) R^(4e) R^(5rr) R^(6b) N250 R^(1b) R^(3q) R^(4e) R^(5rr) R^(6b) N251 R^(1b) R^(3q) R^(4e) R^(5rr) R^(6b) N252 R^(1b) R^(3r) R^(4e) R^(5rr) R^(6b) N253 R^(1b) R^(3r) R^(4e) R^(5rr) R^(6b) N254 R^(1b) R^(3s) R^(4a) R^(5ss) R^(6b) N255 R^(1b) R^(3t) R^(4b) R^(5ss) R^(6b) N256 R^(1b) R^(3g) R^(4e) R^(5ss) R^(6b) N257 R^(1b) R^(3h) R^(4e) R^(5ss) R^(6b) N258 R^(1b) R^(3s) R^(4a) R^(5tt) R^(6b) N259 R^(1b) R^(3t) R^(4b) R^(5tt) R^(6b) N260 R^(1b) R^(3g) R^(4e) R^(5tt) R^(6b) N261 R^(1b) R^(3h) R^(4e) R^(5tt) R^(6b) N262 R^(1b) R^(3s) R^(4a) R^(5uu) R^(6b) N263 R^(1b) R^(3t) R^(4b) R^(5uu) R^(6b) N264 R^(1b) R^(3g) R^(4e) R^(5uu) R^(6b) N265 R^(1b) R^(3h) R^(4e) R^(5uu) R^(6b) N266 R^(1b) R^(3s) R^(4a) R^(5vv) R^(6b) N267 R^(1b) R^(3t) R^(4b) R^(5vv) R^(6b) N268 R^(1b) R^(3g) R^(4e) R^(5vv) R^(6b) N269 R^(1b) R^(3h) R^(4e) R^(5vv) R^(6b) N270 R^(1b) R^(3s) R^(4a) R^(5ww) R^(6b) N271 R^(1b) R^(3t) R^(4b) R^(5ww) R^(6b) N272 R^(1b) R^(3g) R^(4e) R^(5ww) R^(6b) N273 R^(1b) R^(3h) R^(4e) R^(5ww) R^(6b) N274 R^(1b) R^(3s) R^(4a) R^(5xx) R^(6b) N275 R^(1b) R^(3t) R^(4b) R^(5xx) R^(6b) N276 R^(1b) R^(3g) R^(4e) R^(5xx) R^(6b) N277 R^(1b) R^(3h) R^(4e) R^(5xx) R^(6b) N278 R^(1b) R^(3s) R^(4a) R^(5zz) R^(6b) N279 R^(1b) R^(3t) R^(4b) R^(5zz) R^(6b) N280 R^(1b) R^(3g) R^(4e) R^(5zz) R^(6b) N281 R^(1b) R^(3h) R^(4e) R^(5zz) R^(6b) N282 R^(1b) R^(3s) R^(4a) R^(5ba) R^(6b) N283 R^(1b) R^(3t) R^(4b) R^(5ba) R^(6b) N284 R^(1b) R^(3g) R^(4e) R^(5ba) R^(6b) N285 R^(1b) R^(3h) R^(4e) R^(5ba) R^(6b) N286 R^(1b) R^(3s) R^(4a) R^(5bc) R^(6b) N287 R^(1b) R^(3t) R^(4b) R^(5bc) R^(6b) N288 R^(1b) R^(3g) R^(4e) R^(5bc) R^(6b) N289 R^(1b) R^(3h) R^(4e) R^(5bc) R^(6b) N290 R^(1b) R^(3s) R^(4a) R^(5bd) R^(6b) N291 R^(1b) R^(3t) R^(4b) R^(5bd) R^(6b) N292 R^(1b) R^(3g) R^(4e) R^(5bd) R^(6b) N293 R^(1b) R^(3h) R^(4e) R^(5bd) R^(6b) N294 R^(1b) R^(3s) R^(4a) R^(5be) R^(6b) N295 R^(1b) R^(3t) R^(4b) R^(5be) R^(6b) N296 R^(1b) R^(3g) R^(4e) R^(5be) R^(6b) N297 R^(1b) R^(3h) R^(4e) R^(5be) R^(6b) N298 R^(1b) R^(3s) R^(4a) R^(5bf) R^(6b) N299 R^(1b) R^(3t) R^(4b) R^(5bf) R^(6b) N300 R^(1b) R^(3g) R^(4e) R^(5bf) R^(6b) N301 R^(1b) R^(3h) R^(4e) R^(5bf) R^(6b) N302 R^(1b) R^(3s) R^(4a) R^(5bg) R^(6b) N303 R^(1b) R^(3t) R^(4b) R^(5bg) R^(6b) N304 R^(1b) R^(3g) R^(4e) R^(5bg) R^(6b) N305 R^(1b) R^(3h) R^(4e) R^(5bg) R^(6b) N306 R^(1b) R^(3s) R^(4a) R^(5bh) R^(6b) N307 R^(1b) R^(3t) R^(4b) R^(5bh) R^(6b) N308 R^(1b) R^(3g) R^(4e) R^(5bh) R^(6b) N309 R^(1b) R^(3h) R^(4e) R^(5bh) R^(6b) N310 R^(1b) R^(3s) R^(4a) R^(5bi) R^(6b) N311 R^(1b) R^(3t) R^(4b) R^(5bi) R^(6b) N312 R^(1b) R^(3g) R^(4e) R^(5bi) R^(6b) N313 R^(1b) R^(3h) R^(4e) R^(5bi) R^(6b) N314 R^(1b) R^(3s) R^(4a) R^(5bj) R^(6b) N315 R^(1b) R^(3t) R^(4b) R^(5bj) R^(6b) N316 R^(1b) R^(3g) R^(4e) R^(5bj) R^(6b) N317 R^(1b) R^(3h) R^(4e) R^(5bj) R^(6b) N318 R^(1b) R^(3s) R^(4a) R^(5bk) R^(6b) N319 R^(1b) R^(3t) R^(4b) R^(5bk) R^(6b) N320 R^(1b) R^(3g) R^(4e) R^(5bk) R^(6b) N321 R^(1b) R^(3h) R^(4e) R^(5bk) R^(6b) N322 R^(1b) R^(3s) R^(4a) R^(5bl) R^(6b) N323 R^(1b) R^(3t) R^(4b) R^(5bl) R^(6b) N324 R^(1b) R^(3g) R^(4e) R^(5bl) R^(6b) N325 R^(1b) R^(3h) R^(4e) R^(5bl) R^(6b) N326 R^(1b) R^(3s) R^(4a) R^(5bm) R^(6b) N327 R^(1b) R^(3t) R^(4b) R^(5bm) R^(6b) N328 R^(1b) R^(3g) R^(4e) R^(5bm) R^(6b) N329 R^(1b) R^(3h) R^(4e) R^(5bm) R^(6b) N330 R^(1b) R^(3s) R^(4a) R^(5bn) R^(6b) N331 R^(1b) R^(3t) R^(4b) R^(5bn) R^(6b) N332 R^(1b) R^(3g) R^(4e) R^(5bn) R^(6b) N333 R^(1b) R^(3h) R^(4e) R^(5bn) R^(6b) N334 R^(1b) R^(3s) R^(4a) R^(5bo) R^(6b) N335 R^(1b) R^(3t) R^(4b) R^(5bo) R^(6b) N336 R^(1b) R^(3g) R^(4e) R^(5bo) R^(6b) N337 R^(1b) R^(3h) R^(4e) R^(5bo) R^(6b) N338 R^(1b) R^(3s) R^(4a) R^(5bp) R^(6b) N339 R^(1b) R^(3t) R^(4b) R^(5bp) R^(6b) N340 R^(1b) R^(3g) R^(4e) R^(5bp) R^(6b) N341 R^(1b) R^(3h) R^(4e) R^(5bp) R^(6b) N342 R^(1b) R^(3s) R^(4a) R^(5bq) R^(6b) N343 R^(1b) R^(3t) R^(4b) R^(5bq) R^(6b) N344 R^(1b) R^(3g) R^(4e) R^(5bq) R^(6b) N345 R^(1b) R^(3h) R^(4e) R^(5bq) R^(6b) N346 R^(1b) R^(3s) R^(4a) R^(5br) R^(6b) N347 R^(1b) R^(3t) R^(4b) R^(5bq) R^(6b) N348 R^(1b) R^(3g) R^(4e) R^(5bq) R^(6b) N349 R^(1b) R^(3h) R^(4e) R^(5bq) R^(6b) N350 R^(1b) R^(3s) R^(4a) R^(5bs) R^(6b) N351 R^(1b) R^(3t) R^(4b) R^(5bs) R^(6b) N352 R^(1b) R^(3g) R^(4e) R^(5bs) R^(6b) N353 R^(1b) R^(3h) R^(4e) R^(5bs) R^(6b) N354 R^(1b) R^(3s) R^(4a) R^(5bt) R^(6b) N355 R^(1b) R^(3t) R^(4b) R^(5bt) R^(6b) N356 R^(1b) R^(3g) R^(4e) R^(5bt) R^(6b) N357 R^(1b) R^(3h) R^(4e) R^(5bt) R^(6b) N358 R^(1b) R^(3s) R^(4a) R^(5bu) R^(6b) N359 R^(1b) R^(3t) R^(4b) R^(5bu) R^(6b) N360 R^(1b) R^(3g) R^(4e) R^(5bu) R^(6b) N361 R^(1b) R^(3h) R^(4e) R^(5bu) R^(6b) N362 R^(1b) R^(3s) R^(4a) R^(5bv) R^(6b) N363 R^(1b) R^(3t) R^(4b) R^(5bv) R^(6b) N364 R^(1b) R^(3g) R^(4e) R^(5bv) R^(6b) N365 R^(1b) R^(3h) R^(4e) R^(5bv) R^(6b) N366 R^(1b) R^(3s) R^(4a) R^(5bw) R^(6b) N367 R^(1b) R^(3t) R^(4b) R^(5bw) R^(6b) N368 R^(1b) R^(3g) R^(4e) R^(5bw) R^(6b) N369 R^(1b) R^(3h) R^(4e) R^(5bw) R^(6b) N370 R^(1b) R^(3s) R^(4a) R^(5bx) R^(6b) N371 R^(1b) R^(3t) R^(4b) R^(5bx) R^(6b) N372 R^(1b) R^(3g) R^(4e) R^(5bx) R^(6b) N373 R^(1b) R^(3h) R^(4e) R^(5bx) R^(6b) N374 R^(1b) R^(3s) R^(4a) R^(5by) R^(6b) N375 R^(1b) R^(3t) R^(4b) R^(5by) R^(6b) N376 R^(1b) R^(3g) R^(4e) R^(5by) R^(6b) N377 R^(1b) R^(3h) R^(4e) R^(5by) R^(6b) N378 R^(1b) R^(3s) R^(4a) R^(5bz) R^(6b) N379 R^(1b) R^(3t) R^(4b) R^(5bz) R^(6b) N380 R^(1b) R^(3g) R^(4e) R^(5bz) R^(6b) N381 R^(1b) R^(3h) R^(4e) R^(5bz) R^(6b) N382 R^(1b) R^(3s) R^(4a) R^(5ca) R^(6b) N383 R^(1b) R^(3t) R^(4b) R^(5ca) R^(6b) N384 R^(1b) R^(3g) R^(4e) R^(5ca) R^(6b) N385 R^(1b) R^(3h) R^(4e) R^(5ca) R^(6b) N386 R^(1b) R^(3s) R^(4a) R^(5cb) R^(6b) N387 R^(1b) R^(3t) R^(4b) R^(5cb) R^(6b) N388 R^(1b) R^(3g) R^(4e) R^(5cb) R^(6b) N389 R^(1b) R^(3h) R^(4e) R^(5cb) R^(6b) N390 R^(1b) R^(3s) R^(4a) R^(5cd) R^(6b) N391 R^(1b) R^(3t) R^(4b) R^(5cd) R^(6b) N392 R^(1b) R^(3g) R^(4e) R^(5cd) R^(6b) N393 R^(1b) R^(3h) R^(4e) R^(5cd) R^(6b) N394 R^(1b) R^(3s) R^(4a) R^(5ce) R^(6b) N395 R^(1b) R^(3t) R^(4b) R^(5ce) R^(6b) N396 R^(1b) R^(3g) R^(4e) R^(5ce) R^(6b) N397 R^(1b) R^(3h) R^(4e) R^(5ce) R^(6b) N398 R^(1b) R^(3s) R^(4a) R^(5cf) R^(6b) N399 R^(1b) R^(3t) R^(4b) R^(5cf) R^(6b) N400 R^(1b) R^(3g) R^(4e) R^(5cf) R^(6b) N401 R^(1b) R^(3h) R^(4e) R^(5cf) R^(6b) N402 R^(1b) R^(3s) R^(4a) R^(5cg) R^(6b) N403 R^(1b) R^(3t) R^(4b) R^(5cg) R^(6b) N404 R^(1b) R^(3g) R^(4e) R^(5cg) R^(6b) N405 R^(1b) R^(3h) R^(4e) R^(5cg) R^(6b) N406 R^(1b) R^(3s) R^(4a) R^(5ch) R^(6b) N407 R^(1b) R^(3t) R^(4b) R^(5ch) R^(6b) N408 R^(1b) R^(3g) R^(4e) R^(5ch) R^(6b) N409 R^(1b) R^(3h) R^(4e) R^(5ch) R^(6b) N410 R^(1b) R^(3s) R^(4a) R^(5ci) R^(6b) N411 R^(1b) R^(3t) R^(4b) R^(5ci) R^(6b) N412 R^(1b) R^(3g) R^(4e) R^(5ci) R^(6b) N413 R^(1b) R^(3h) R^(4e) R^(5ci) R^(6b) N414 R^(1b) R^(3s) R^(4a) R^(5cj) R^(6b) N415 R^(1b) R^(3t) R^(4b) R^(5cj) R^(6b) N416 R^(1b) R^(3g) R^(4e) R^(5cj) R^(6b) N417 R^(1b) R^(3h) R^(4e) R^(5cj) R^(6b) N418 R^(1b) R^(3s) R^(4a) R^(5ck) R^(6b) N419 R^(1b) R^(3t) R^(4b) R^(5ck) R^(6b) N420 R^(1b) R^(3g) R^(4e) R^(5ck) R^(6b) N421 R^(1b) R^(3h) R^(4e) R^(5ck) R^(6b) N422 R^(1b) R^(3s) R^(4a) R^(5cl) R^(6b) N423 R^(1b) R^(3t) R^(4b) R^(5cl) R^(6b) N424 R^(1b) R^(3g) R^(4e) R^(5cl) R^(6b) N425 R^(1b) R^(3h) R^(4e) R^(5cl) R^(6b) N426 R^(1b) R^(3s) R^(4a) R^(5cm) R^(6b) N427 R^(1b) R^(3t) R^(4b) R^(5cm) R^(6b) N428 R^(1b) R^(3g) R^(4e) R^(5cm) R^(6b) N429 R^(1b) R^(3h) R^(4e) R^(5cm) R^(6b) N430 R^(1b) R^(3s) R^(4a) R^(5cn) R^(6b) N431 R^(1b) R^(3t) R^(4b) R^(5cn) R^(6b) N432 R^(1b) R^(3g) R^(4e) R^(5cn) R^(6b) N433 R^(1b) R^(3h) R^(4e) R^(5cn) R^(6b) N434 R^(1b) R^(3s) R^(4a) R^(5co) R^(6b) N435 R^(1b) R^(3t) R^(4b) R^(5co) R^(6b) N436 R^(1b) R^(3g) R^(4e) R^(5co) R^(6b) N437 R^(1b) R^(3h) R^(4e) R^(5co) R^(6b) N438 R^(1b) R^(3s) R^(4a) R^(5cp) R^(6b) N439 R^(1b) R^(3t) R^(4b) R^(5cp) R^(6b) N440 R^(1b) R^(3g) R^(4e) R^(5cp) R^(6b) N441 R^(1b) R^(3h) R^(4e) R^(5cp) R^(6b) N442 R^(1b) R^(3s) R^(4a) R^(5cq) R^(6b) N443 R^(1b) R^(3t) R^(4b) R^(5cq) R^(6b) N444 R^(1b) R^(3g) R^(4e) R^(5cq) R^(6b) N445 R^(1b) R^(3h) R^(4e) R^(5cq) R^(6b) N446 R^(1b) R^(3s) R^(4a) R^(5cr) R^(6b) N447 R^(1b) R^(3t) R^(4b) R^(5cr) R^(6b) N448 R^(1b) R^(3g) R^(4e) R^(5cr) R^(6b) N449 R^(1b) R^(3h) R^(4e) R^(5cr) R^(6b) N450 R^(1b) R^(3s) R^(4a) R^(5cs) R^(6b) N451 R^(1b) R^(3t) R^(4b) R^(5cs) R^(6b) N452 R^(1b) R^(3g) R^(4e) R^(5cs) R^(6b) N453 R^(1b) R^(3h) R^(4e) R^(5cs) R^(6b) N454 R^(1b) R^(3s) R^(4a) R^(5ct) R^(6b) N455 R^(1b) R^(3t) R^(4b) R^(5ct) R^(6b) N456 R^(1b) R^(3g) R^(4e) R^(5ct) R^(6b) N457 R^(1b) R^(3h) R^(4e) R^(5ct) R^(6b) N458 R^(1b) R^(3s) R^(4a) R^(5cu) R^(6b) N459 R^(1b) R^(3t) R^(4b) R^(5cu) R^(6b) N460 R^(1b) R^(3g) R^(4e) R^(5cu) R^(6b) N461 R^(1b) R^(3h) R^(4e) R^(5cu) R^(6b) N462 R^(1b) R^(3s) R^(4a) R^(5cv) R^(6b) N463 R^(1b) R^(3t) R^(4b) R^(5cv) R^(6b) N464 R^(1b) R^(3g) R^(4e) R^(5cv) R^(6b) N465 R^(1b) R^(3h) R^(4e) R^(5cv) R^(6b) N466 R^(1b) R^(3s) R^(4a) R^(5cw) R^(6b) N467 R^(1b) R^(3t) R^(4b) R^(5cw) R^(6b) N468 R^(1b) R^(3g) R^(4e) R^(5cw) R^(6b) N469 R^(1b) R^(3h) R^(4e) R^(5cw) R^(6b) N470 R^(1b) R^(3s) R^(4a) R^(5cx) R^(6b) N471 R^(1b) R^(3t) R^(4b) R^(5cx) R^(6b) N472 R^(1b) R^(3g) R^(4e) R^(5cx) R^(6b) N473 R^(1b) R^(3h) R^(4e) R^(5cx) R^(6b) N474 R^(1b) R^(3s) R^(4a) R^(5cy) R^(6b) N475 R^(1b) R^(3t) R^(4b) R^(5cy) R^(6b) N476 R^(1b) R^(3g) R^(4e) R^(5cy) R^(6b) N477 R^(1b) R^(3h) R^(4e) R^(5cy) R^(6b) N478 R^(1b) R^(3s) R^(4a) R^(5cz) R^(6b) N479 R^(1b) R^(3t) R^(4b) R^(5cz) R^(6b) N480 R^(1b) R^(3g) R^(4e) R^(5cz) R^(6b) N481 R^(1b) R^(3h) R^(4e) R^(5cz) R^(6b) N482 R^(1b) R^(3s) R^(4a) R^(5da) R^(6b) N483 R^(1b) R^(3t) R^(4b) R^(5da) R^(6b) N484 R^(1b) R^(3g) R^(4e) R^(5da) R^(6b) N485 R^(1b) R^(3h) R^(4e) R^(5da) R^(6b) N486 R^(1b) R^(3s) R^(4a) R^(5db) R^(6b) N487 R^(1b) R^(3t) R^(4b) R^(5db) R^(6b) N488 R^(1b) R^(3g) R^(4e) R^(5db) R^(6b) N489 R^(1b) R^(3h) R^(4e) R^(5db) R^(6b) N490 R^(1b) R^(3s) R^(4a) R^(5dc) R^(6b) N491 R^(1b) R^(3t) R^(4b) R^(5dc) R^(6b) N492 R^(1b) R^(3g) R^(4e) R^(5dc) R^(6b) N493 R^(1b) R^(3h) R^(4e) R^(5dc) R^(6b) N494 R^(1b) R^(3s) R^(4a) R^(5de) R^(6b) N495 R^(1b) R^(3t) R^(4b) R^(5de) R^(6b) N496 R^(1b) R^(3g) R^(4e) R^(5de) R^(6b) N497 R^(1b) R^(3h) R^(4e) R^(5de) R^(6b) N498 R^(1b) R^(3s) R^(4a) R^(5df) R^(6b) N499 R^(1b) R^(3t) R^(4b) R^(5df) R^(6b) N500 R^(1b) R^(3g) R^(4e) R^(5df) R^(6b) N501 R^(1b) R^(3h) R^(4e) R^(5df) R^(6b) N502 R^(1b) R^(3s) R^(4a) R^(5dg) R^(6b) N503 R^(1b) R^(3t) R^(4b) R^(5dg) R^(6b) N504 R^(1b) R^(3g) R^(4e) R^(5dg) R^(6b) N505 R^(1b) R^(3h) R^(4e) R^(5dg) R^(6b) N506 R^(1b) R^(3s) R^(4a) R^(5dh) R^(6b) N507 R^(1b) R^(3t) R^(4b) R^(5dh) R^(6b) N508 R^(1b) R^(3g) R^(4e) R^(5dh) R^(6b) N509 R^(1b) R^(3h) R^(4e) R^(5dh) R^(6b) N510 R^(1b) R^(3s) R^(4a) R^(5di) R^(6b) N511 R^(1b) R^(3t) R^(4b) R^(5di) R^(6b) N512 R^(1b) R^(3g) R^(4e) R^(5di) R^(6b) N513 R^(1b) R^(3h) R^(4e) R^(5di) R^(6b) N514 R^(1b) R^(3s) R^(4a) R^(5dj) R^(6b) N515 R^(1b) R^(3t) R^(4b) R^(5dj) R^(6b) N516 R^(1b) R^(3g) R^(4e) R^(5dj) R^(6b) N517 R^(1b) R^(3h) R^(4e) R^(5dj) R^(6b) N518 R^(1b) R^(3s) R^(4a) R^(5dk) R^(6b) N519 R^(1b) R^(3t) R^(4b) R^(5dk) R^(6b) N520 R^(1b) R^(3g) R^(4e) R^(5dk) R^(6b) N521 R^(1b) R^(3h) R^(4e) R^(5dk) R^(6b) N522 R^(1b) R^(3s) R^(4a) R^(5dl) R^(6b) N523 R^(1b) R^(3t) R^(4b) R^(5dl) R^(6b) N524 R^(1b) R^(3g) R^(4e) R^(5dl) R^(6b) N525 R^(1b) R^(3h) R^(4e) R^(5dl) R^(6b) N526 R^(1b) R^(3s) R^(4a) R^(5dm) R^(6b) N527 R^(1b) R^(3t) R^(4b) R^(5dm) R^(6b) N528 R^(1b) R^(3g) R^(4e) R^(5dm) R^(6b) N529 R^(1b) R^(3h) R^(4e) R^(5dm) R^(6b) N530 R^(1b) R^(3s) R^(4a) R^(5dn) R^(6b) N531 R^(1b) R^(3t) R^(4b) R^(5dn) R^(6b) N532 R^(1b) R^(3g) R^(4e) R^(5dn) R^(6b) N533 R^(1b) R^(3h) R^(4e) R^(5dn) R^(6b) N534 R^(1b) R^(3s) R^(4a) R^(5do) R^(6b) N535 R^(1b) R^(3t) R^(4b) R^(5do) R^(6b) N536 R^(1b) R^(3g) R^(4e) R^(5do) R^(6b) N537 R^(1b) R^(3h) R^(4e) R^(5do) R^(6b) N538 R^(1b) R^(3s) R^(4a) R^(5dp) R^(6b) N539 R^(1b) R^(3t) R^(4b) R^(5dp) R^(6b) N540 R^(1b) R^(3g) R^(4e) R^(5dp) R^(6b) N541 R^(1b) R^(3h) R^(4e) R^(5dp) R^(6b) N542 R^(1b) R^(3s) R^(4a) R^(5dq) R^(6b) N543 R^(1b) R^(3t) R^(4b) R^(5dq) R^(6b) N544 R^(1b) R^(3g) R^(4e) R^(5dq) R^(6b) N545 R^(1b) R^(3h) R^(4e) R^(5dq) R^(6b) N546 R^(1b) R^(3s) R^(4a) R^(5dr) R^(6b) N547 R^(1b) R^(3t) R^(4b) R^(5dr) R^(6b) N548 R^(1b) R^(3g) R^(4e) R^(5dr) R^(6b) N549 R^(1b) R^(3h) R^(4e) R^(5dr) R^(6b) N550 R^(1b) R^(3s) R^(4a) R^(5ds) R^(6b) N551 R^(1b) R^(3t) R^(4b) R^(5ds) R^(6b) N552 R^(1b) R^(3g) R^(4e) R^(5ds) R^(6b) N553 R^(1b) R^(3h) R^(4e) R^(5ds) R^(6b) N554 R^(1b) R^(3s) R^(4a) R^(5dt) R^(6b) N555 R^(1b) R^(3t) R^(4b) R^(5dt) R^(6b) N556 R^(1b) R^(3g) R^(4e) R^(5dt) R^(6b) N557 R^(1b) R^(3h) R^(4e) R^(5dt) R^(6b) N558 R^(1b) R^(3s) R^(4a) R^(5du) R^(6b) N559 R^(1b) R^(3t) R^(4b) R^(5du) R^(6b) N560 R^(1b) R^(3g) R^(4e) R^(5du) R^(6b) N561 R^(1b) R^(3h) R^(4e) R^(5du) R^(6b) N562 R^(1b) R^(3s) R^(4a) R^(5dv) R^(6b) N563 R^(1b) R^(3t) R^(4b) R^(5dv) R^(6b) N564 R^(1b) R^(3g) R^(4e) R^(5dv) R^(6b) N565 R^(1b) R^(3h) R^(4e) R^(5dv) R^(6b) N566 R^(1b) R^(3s) R^(4a) R^(5dw) R^(6b) N567 R^(1b) R^(3t) R^(4b) R^(5dw) R^(6b) N568 R^(1b) R^(3g) R^(4e) R^(5dw) R^(6b) N569 R^(1b) R^(3h) R^(4e) R^(5dw) R^(6b) N570 R^(1b) R^(3s) R^(4a) R^(5dx) R^(6b) N571 R^(1b) R^(3t) R^(4b) R^(5dx) R^(6b) N572 R^(1b) R^(3g) R^(4e) R^(5dx) R^(6b) N573 R^(1b) R^(3h) R^(4e) R^(5dx) R^(6b) N574 R^(1b) R^(3s) R^(4a) R^(5ea) R^(6b) N575 R^(1b) R^(3t) R^(4b) R^(5ea) R^(6b) N576 R^(1b) R^(3g) R^(4e) R^(5ea) R^(6b) N577 R^(1b) R^(3h) R^(4e) R^(5ea) R^(6b) N578 R^(1b) R^(3s) R^(4a) R^(5eb) R^(6b) N579 R^(1b) R^(3t) R^(4b) R^(5eb) R^(6b) N580 R^(1b) R^(3g) R^(4e) R^(5eb) R^(6b) N581 R^(1b) R^(3h) R^(4e) R^(5eb) R^(6b) N582 R^(1b) R^(3s) R^(4a) R^(5ec) R^(6b) N583 R^(1b) R^(3t) R^(4b) R^(5ec) R^(6b) N584 R^(1b) R^(3g) R^(4e) R^(5ec) R^(6b) N585 R^(1b) R^(3h) R^(4e) R^(5ec) R^(6b) N586 R^(1b) R^(3s) R^(4a) R^(5ed) R^(6b) N587 R^(1b) R^(3t) R^(4b) R^(5ed) R^(6b) N588 R^(1b) R^(3g) R^(4e) R^(5ed) R^(6b) N589 R^(1b) R^(3h) R^(4e) R^(5ed) R^(6b) N590 R^(1b) R^(3s) R^(4a) R^(5ef) R^(6b) N591 R^(1b) R^(3t) R^(4b) R^(5ef) R^(6b) N592 R^(1b) R^(3g) R^(4e) R^(5ef) R^(6b) N593 R^(1b) R^(3h) R^(4e) R^(5ef) R^(6b) N594 R^(1b) R^(3s) R^(4a) R^(5eg) R^(6b) N595 R^(1b) R^(3t) R^(4b) R^(5eg) R^(6b) N596 R^(1b) R^(3g) R^(4e) R^(5eg) R^(6b) N597 R^(1b) R^(3h) R^(4e) R^(5eg) R^(6b) N598 R^(1b) R^(3s) R^(4a) R^(5eh) R^(6b) N599 R^(1b) R^(3t) R^(4b) R^(5eh) R^(6b) N600 R^(1b) R^(3g) R^(4e) R^(5eh) R^(6b) N601 R^(1b) R^(3h) R^(4e) R^(5eh) R^(6b) N602 R^(1b) R^(3s) R^(4a) R^(5ei) R^(6b) N603 R^(1b) R^(3t) R^(4b) R^(5ei) R^(6b) N604 R^(1b) R^(3g) R^(4e) R^(5ei) R^(6b) N605 R^(1b) R^(3h) R^(4e) R^(5ei) R^(6b) N606 R^(1b) R^(3s) R^(4a) R^(5ej) R^(6b) N607 R^(1b) R^(3t) R^(4b) R^(5ej) R^(6b) N608 R^(1b) R^(3g) R^(4e) R^(5ej) R^(6b) N609 R^(1b) R^(3h) R^(4e) R^(5ej) R^(6b) N610 R^(1b) R^(3s) R^(4a) R^(5ek) R^(6b) N611 R^(1b) R^(3t) R^(4b) R^(5ej) R^(6b) N612 R^(1b) R^(3g) R^(4e) R^(5ej) R^(6b) N613 R^(1b) R^(3h) R^(4e) R^(5ej) R^(6b) N614 R^(1b) R^(3s) R^(4a) R^(5el) R^(6b) N615 R^(1b) R^(3t) R^(4b) R^(5el) R^(6b) N616 R^(1b) R^(3g) R^(4e) R^(5el) R^(6b) N617 R^(1b) R^(3h) R^(4e) R^(5el) R^(6b) N618 R^(1b) R^(3s) R^(4a) R^(5em) R^(6b) N619 R^(1b) R^(3t) R^(4b) R^(5em) R^(6b) N620 R^(1b) R^(3g) R^(4e) R^(5em) R^(6b) N621 R^(1b) R^(3h) R^(4e) R^(5em) R^(6b) N622 R^(1b) R^(3s) R^(4a) R^(5en) R^(6b) N623 R^(1b) R^(3t) R^(4b) R^(5en) R^(6b) N624 R^(1b) R^(3g) R^(4e) R^(5en) R^(6b) N625 R^(1b) R^(3h) R^(4e) R^(5en) R^(6b) N626 R^(1b) R^(3s) R^(4a) R^(5eo) R^(6b) N627 R^(1b) R^(3t) R^(4b) R^(5eo) R^(6b) N628 R^(1b) R^(3g) R^(4e) R^(5eo) R^(6b) N629 R^(1b) R^(3h) R^(4e) R^(5eo) R^(6b) N630 R^(1b) R^(3s) R^(4a) R^(5ep) R^(6b) N631 R^(1b) R^(3t) R^(4b) R^(5ep) R^(6b) N632 R^(1b) R^(3g) R^(4e) R^(5ep) R^(6b) N633 R^(1b) R^(3h) R^(4e) R^(5ep) R^(6b) N634 R^(1b) R^(3s) R^(4a) R^(5eq) R^(6b) N635 R^(1b) R^(3t) R^(4b) R^(5eq) R^(6b) N636 R^(1b) R^(3q) R^(4e) R^(5eq) R^(6b) N637 R^(1b) R^(3h) R^(4e) R^(5eq) R^(6b) N638 R^(1b) R^(3s) R^(4a) R^(5er) R^(6b) N639 R^(1b) R^(3t) R^(4b) R^(5er) R^(6b) N640 R^(1b) R^(3g) R^(4e) R^(5er) R^(6b) N641 R^(1b) R^(3h) R^(4e) R^(5er) R^(6b) N642 R^(1b) R^(3s) R^(4a) R^(5es) R^(6b) N643 R^(1b) R^(3t) R^(4b) R^(5es) R^(6b) N644 R^(1b) R^(3g) R^(4e) R^(5es) R^(6b) N645 R^(1b) R^(3h) R^(4e) R^(5es) R^(6b) N646 R^(1b) R^(3s) R^(4a) R^(5et) R^(6b) N647 R^(1b) R^(3t) R^(4b) R^(5et) R^(6b) N648 R^(1b) R^(3g) R^(4e) R^(5et) R^(6b) N649 R^(1b) R^(3h) R^(4e) R^(5et) R^(6b) N650 R^(1b) R^(3s) R^(4a) R^(5eu) R^(6b) N651 R^(1b) R^(3t) R^(4b) R^(5eu) R^(6b) N652 R^(1b) R^(3g) R^(4e) R^(5eu) R^(6b) N653 R^(1b) R^(3h) R^(4e) R^(5eu) R^(6b) N654 R^(1b) R^(3s) R^(4a) R^(5ev) R^(6b) N655 R^(1b) R^(3t) R^(4b) R^(5ev) R^(6b) N656 R^(1b) R^(3g) R^(4e) R^(5ev) R^(6b) N657 R^(1b) R^(3h) R^(4e) R^(5ev) R^(6b) N658 R^(1b) R^(3s) R^(4a) R^(5ex) R^(6b) N659 R^(1b) R^(3t) R^(4b) R^(5ex) R^(6b) N660 R^(1b) R^(3g) R^(4e) R^(5ex) R^(6b) N661 R^(1b) R^(3h) R^(4e) R^(5ex) R^(6b) N662 R^(1b) R^(3s) R^(4a) R^(5ey) R^(6b) N663 R^(1b) R^(3t) R^(4b) R^(5ey) R^(6b) N664 R^(1b) R^(3g) R^(4e) R^(5ey) R^(6b) N665 R^(1b) R^(3h) R^(4e) R^(5ey) R^(6b) N666 R^(1b) R^(3s) R^(4a) R^(5ez) R^(6b) N667 R^(1b) R^(3t) R^(4b) R^(5ez) R^(6b) N668 R^(1b) R^(3g) R^(4e) R^(5ez) R^(6b) N669 R^(1b) R^(3h) R^(4e) R^(5ez) R^(6b) N670 R^(1b) R^(3s) R^(4a) R^(5fa) R^(6b) N671 R^(1b) R^(3t) R^(4b) R^(5fa) R^(6b) N672 R^(1b) R^(3g) R^(4e) R^(5fa) R^(6b) N673 R^(1b) R^(3h) R^(4e) R^(5fa) R^(6b) N674 R^(1b) R^(3s) R^(4a) R^(5fb) R^(6b) N675 R^(1b) R^(3t) R^(4b) R^(5fb) R^(6b) N676 R^(1b) R^(3g) R^(4e) R^(5fb) R^(6b) N677 R^(1b) R^(3h) R^(4e) R^(5fb) R^(6b) N678 R^(1b) R^(3s) R^(4a) R^(5fc) R^(6b) N679 R^(1b) R^(3t) R^(4b) R^(5fc) R^(6b) N680 R^(1b) R^(3g) R^(4e) R^(5fc) R^(6b) N681 R^(1b) R^(3h) R^(4e) R^(5fc) R^(6b) N682 R^(1b) R^(3s) R^(4a) R^(5fd) R^(6b) N683 R^(1b) R^(3t) R^(4b) R^(5fd) R^(6b) N684 R^(1b) R^(3g) R^(4e) R^(5fd) R^(6b) N685 R^(1b) R^(3h) R^(4e) R^(5fd) R^(6b) N686 R^(1b) R^(3s) R^(4a) R^(5fe) R^(6b) N687 R^(1b) R^(3t) R^(4b) R^(5fe) R^(6b) N688 R^(1b) R^(3g) R^(4e) R^(5fe) R^(6b) N689 R^(1b) R^(3h) R^(4e) R^(5fe) R^(6b) N690 R^(1b) R^(3s) R^(4a) R^(5fg) R^(6b) N691 R^(1b) R^(3t) R^(4b) R^(5fg) R^(6b) N692 R^(1b) R^(3g) R^(4e) R^(5fg) R^(6b) N693 R^(1b) R^(3h) R^(4e) R^(5fg) R^(6b) N694 R^(1b) R^(3s) R^(4a) R^(5fh) R^(6b) N695 R^(1b) R^(3t) R^(4b) R^(5fh) R^(6b) N696 R^(1b) R^(3g) R^(4e) R^(5fh) R^(6b) N697 R^(1b) R^(3h) R^(4e) R^(5fh) R^(6b) N698 R^(1b) R^(3s) R^(4a) R^(5fh) R^(6b) N699 R^(1b) R^(3t) R^(4b) R^(5fi) R^(6b) N700 R^(1b) R^(3g) R^(4e) R^(5fi) R^(6b) N701 R^(1b) R^(3h) R^(4e) R^(5fi) R^(6b) N702 R^(1b) R^(3s) R^(4a) R^(5fj) R^(6b) N703 R^(1b) R^(3t) R^(4b) R^(5fj) R^(6b) N704 R^(1b) R^(3g) R^(4e) R^(5fj) R^(6b) N705 R^(1b) R^(3h) R^(4e) R^(5fj) R^(6b) N706 R^(1b) R^(3s) R^(4a) R^(5fk) R^(6b) N707 R^(1b) R^(3t) R^(4b) R^(5fk) R^(6b) N708 R^(1b) R^(3g) R^(4e) R^(5fk) R^(6b) N709 R^(1b) R^(3h) R^(4e) R^(5fk) R^(6b) N710 R^(1b) R^(3s) R^(4a) R^(5fl) R^(6b) N711 R^(1b) R^(3t) R^(4b) R^(5fl) R^(6b) N712 R^(1b) R^(3g) R^(4e) R^(5fl) R^(6b) N713 R^(1b) R^(3h) R^(4e) R^(5fl) R^(6b) N714 R^(1b) R^(3s) R^(4a) R^(5fm) R^(6b) N715 R^(1b) R^(3t) R^(4b) R^(5fm) R^(6b) N716 R^(1b) R^(3g) R^(4e) R^(5fm) R^(6b) N717 R^(1b) R^(3h) R^(4e) R^(5fm) R^(6b) N718 R^(1b) R^(3s) R^(4a) R^(5fn) R^(6b) N719 R^(1b) R^(3t) R^(4b) R^(5fn) R^(6b) N720 R^(1b) R^(3g) R^(4e) R^(5fn) R^(6b) N721 R^(1b) R^(3h) R^(4e) R^(5fn) R^(6b) N722 R^(1b) R^(3s) R^(4a) R^(5fo) R^(6b) N723 R^(1b) R^(3t) R^(4b) R^(5fo) R^(6b) N724 R^(1b) R^(3g) R^(4e) R^(5fo) R^(6b) N725 R^(1b) R^(3h) R^(4e) R^(5fo) R^(6b) N726 R^(1b) R^(3s) R^(4a) R^(5fp) R^(6b) N727 R^(1b) R^(3t) R^(4b) R^(5fp) R^(6b) N728 R^(1b) R^(3g) R^(4e) R^(5fp) R^(6b) N729 R^(1b) R^(3h) R^(4e) R^(5fp) R^(6b) N730 R^(1b) R^(3s) R^(4a) R^(5fq) R^(6b) N731 R^(1b) R^(3t) R^(4b) R^(5fq) R^(6b) N732 R^(1b) R^(3g) R^(4e) R^(5fq) R^(6b) N733 R^(1b) R^(3h) R^(4e) R^(5fq) R^(6b) N734 R^(1b) R^(3s) R^(4a) R^(5fr) R^(6b) N735 R^(1b) R^(3t) R^(4b) R^(5fr) R^(6b) N736 R^(1b) R^(3g) R^(4e) R^(5fr) R^(6b) N737 R^(1b) R^(3h) R^(4e) R^(5fr) R^(6b) N738 R^(1b) R^(3s) R^(4a) R^(5fs) R^(6b) N739 R^(1b) R^(3t) R^(4b) R^(5fs) R^(6b) N740 R^(1b) R^(3g) R^(4e) R^(5fs) R^(6b) N741 R^(1b) R^(3h) R^(4e) R^(5fs) R^(6b) N742 R^(1b) R^(3s) R^(4a) R^(5ft) R^(6b) N743 R^(1b) R^(3t) R^(4b) R^(5ft) R^(6b) N744 R^(1b) R^(3g) R^(4e) R^(5ft) R^(6b) N745 R^(1b) R^(3h) R^(4e) R^(5ft) R^(6b) N746 R^(1b) R^(3s) R^(4a) R^(5fu) R^(6b) N747 R^(1b) R^(3t) R^(4b) R^(5fu) R^(6b) N748 R^(1b) R^(3g) R^(4e) R^(5fu) R^(6b) N749 R^(1b) R^(3h) R^(4e) R^(5fu) R^(6b) N750 R^(1b) R^(3s) R^(4a) R^(5fv) R^(6b) N751 R^(1b) R^(3t) R^(4b) R^(5fv) R^(6b) N752 R^(1b) R^(3g) R^(4e) R^(5fv) R^(6b) N753 R^(1b) R^(3h) R^(4e) R^(5fv) R^(6b) N754 R^(1b) R^(3s) R^(4a) R^(5fw) R^(6b) N755 R^(1b) R^(3t) R^(4b) R^(5fw) R^(6b) N756 R^(1b) R^(3g) R^(4e) R^(5fw) R^(6b) N757 R^(1b) R^(3h) R^(4e) R^(5fw) R^(6b)

Compounds of formula I as well as intermediates and reagents used can be prepared by the methods herein and as described in WO2008/101682 as well as further methods known to a skilled chemist in a variety of ways, or they are commercially available.

In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Chlorothalonil. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fludioxonil. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Cyprodinil. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fenpropidin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Mandipropamid. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fluazinam. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Procymedone. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Carbendazim. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Abamectin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Clothianidin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Emamectin benzoate. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Imidacloprid. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Tefluthrin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Mefenoxam. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Orocymedone. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Thiamethoxam. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Lambda-cyhalothrin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Gamma-cyhalothrin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Profenofos. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Lufenuron. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Diflubenzuron. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Cypermethrin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Novaluron. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Bifenthrin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Methomyl. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Chlopyrifos. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Methamidophos. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Endosulfan. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Betacyfluthrin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Triflumuron. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Teflubenzuron. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Acephat. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Glyphosate. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Glufosinate. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Mesotrione. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Bicyclopyrone. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Tembotrione. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Sulcotrione. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is 2,4-D. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164 or a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is MCPA. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Trinexapac-ethyl. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Prohexadione-Ca. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Paclobutrazol. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Acibenzolar-S-methyl. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Methyl-Jasmonate. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Cis-Jasmone. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Manganese. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Cyflufenamid. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Tebufloquin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Copper. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Coumoxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Dicloaminostrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Flufenoxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Pyrametostrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Pyraoxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Trifloxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Azoxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Pyraclostrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Picoxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Jiaxiangjunzhi. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Enoxastrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Triclopyricarb. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fluoxastrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Dimoxystrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fenaminostrobin. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is the compound of formula II. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Cyproconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Difenoconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Metconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Propiconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Epoxiconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Tebuconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Flutriafol. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Ipconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is 1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol [CAS number 120983-64-4]. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is prothioconazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is (S)-[3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol [CAS number 1229606-46-5]. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164 or a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol [CAS number 1229605-96-2]. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Pyrisoxazole. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-Pyrazole-4-carboxamide [CAS number 1228284-64-7]. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide [CAS number 1072957-71-1]. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Isopyrazam. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Sedaxane. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Boscalid. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fluxapyroxad. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Penthiopyrad. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Penflufen. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Bixafen. In a further preferred embodiment the component A is a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454 and the component B is Fluopyram. In a further embodiment the invention relates to a specific compound selected from Tables 1 to 164, a specific compound selected from P.1 to P.372 or a specific compound selected from Q.001 to Q.454.

The compounds of formula I, and, where appropriate, the tautomers thereof, can be present in the form of one of the isomers which are possible or as a mixture of these, for example in the form of pure isomers, such as antipodes and/or diastereomers, or as isomer mixtures, such as structural isomer, stereo isomer, diastereoisomer and enantiomer mixtures, for example racemates, diastereomer mixtures or racemate mixtures, depending on the number, absolute and relative configuration of asymmetric carbon atoms which occur in the molecule and/or depending on the configuration of non-aromatic double bonds which occur in the molecule; the invention relates to the pure isomers and also to all isomer mixtures which are possible and is to be understood in each case in this sense hereinabove and hereinbelow, even when stereochemical details are not mentioned specifically in each case.

Likewise, where isomers are possible for compounds that may be selected as component B, the invention relates to the pure isomers and also to all isomer mixtures which are possible.

The compositions according to the invention have, for practical purposes, a very advantageous spectrum of activities for protecting useful plants against diseases that are caused by phytopathogenic microorganisms, such as fungi, bacteria or viruses.

The invention relates to a method of controlling or preventing infestation of useful plants by phytopathogenic microorganisms, wherein a composition of the invention is applied to the plants, to parts thereof or the locus thereof. The compositions according to the invention are distinguished by excellent activity at low rates of application, by being well tolerated by plants and by being environmentally safe. They have very useful curative, preventive and systemic properties and are used for protecting numerous useful plants. The compositions of the invention can be used to inhibit or destroy the diseases that occur on plants or parts of plants (fruit, blossoms, leaves, stems, tubers, roots) of different crops of useful plants, while at the same time protecting also those parts of the plants that grow later e.g. from phytopathogenic microorganisms.

It is also possible to use compositions of the invention as dressing agents for the treatment of plant propagation material, in particular of seeds (fruit, tubers, grains) and plant cuttings (e.g. rice), for the protection against fungal infections as well as against phytopathogenic fungi occurring in the soil.

Furthermore the compositions of the invention may be used for controlling fungi in related areas, for example in the protection of technical materials, including wood and wood related technical products, in food storage or in hygiene management.

The compositions of the invention are, for example, effective against the phytopathogenic fungi of the following classes: Fungi imperfecti (e.g. Botrytis, Pyricularia, Helminthosporium, Fusarium, Septoria, Cercospora and Alternaria) and Basidiomycetes (e.g. Rhizoctonia, Hemileia, Puccinia). Additionally, they are also effective against the Ascomycetes classes (e.g. Venturia and Erysiphe, Podosphaera, Monilinia, Uncinula) and of the Oomycetes classes (e.g. Phytophthora, Pythium, Plasmopara). Outstanding activity has been observed against powdery mildew (Erysiphe spp.). Furthermore, the compositions of the invention are effective against phytopathogenic bacteria and viruses (e.g. against Xanthomonas spp, Pseudomonas spp, Erwinia amylovora as well as against the tobacco mosaic virus). Good activity has been observed against rust disease, like leaf rust (Puccinia spp.) and soybean rust (Phakopsora pachyrhizi).

Within the scope of the invention, useful plants to be protected typically comprise the following species of plants: cereal (wheat, barley, rye, oat, rice, maize, sorghum and related species); beet (sugar beet and fodder beet); pomes, drupes and soft fruit (apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries and blackberries); leguminous plants (beans, lentils, peas, soybeans); oil plants (rape, mustard, poppy, olives, sunflowers, coconut, castor oil plants, cocoa beans, groundnuts); cucumber plants (pumpkins, cucum-bers, melons); fiber plants (cotton, flax, hemp, jute); citrus fruit (oranges, lemons, grapefruit, mandarins); vegetables (spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, paprika); lauraceae (avocado, cinnamomum, camphor) or plants such as tobacco, nuts, coffee, eggplants, sugar cane, tea, pepper, vines, hops, bananas and natural rubber plants, as well as ornamentals and turf and grass species.

The toxin contained in the transgenic plants imparts to the plants tolerance to harmful insects. Such insects can occur in any taxonomic group of insects, but are especially commonly found in the beetles (Coleoptera), two-winged insects (Diptera) and butterflies (Lepidoptera).

Transgenic plants containing one or more genes that code for an insecticidal resistance and express one or more toxins are known and some of them are commercially available. Examples of such plants are: YieldGard® (maize variety that expresses a Cry1Ab toxin); YieldGard Rootworm® (maize variety that expresses a Cry3Bb1 toxin); YieldGard Plus® (maize variety that expresses a Cry1Ab and a Cry3Bb1 toxin); Starlink® (maize variety that expresses a Cry9C toxin); Herculex I® (maize variety that expresses a Cry1Fa2 toxin and the enzyme phosphinothricine N-acetyltransferase (PAT) to achieve tolerance to the herbicide glufosinate ammonium); NuCOTN 33B® (cotton variety that expresses a Cry1Ac toxin); Bollgard I® (cotton variety that expresses a Cry1Ac toxin); Bollgard II® (cotton variety that expresses a Cry1Ac and a Cry2Ab toxin); VipCot® (cotton variety that expresses a Vip3A and a Cry1Ab toxin); NewLeaf® (potato variety that expresses a Cry3A toxin); NatureGard®, Agrisure® GT Advantage (GA21 glyphosate-tolerant trait), Agrisure® CB Advantage (Bt11 corn borer (CB) trait) and Protecta®.

Further examples of such transgenic crops are:

1. Bt11 Maize from Syngenta Seeds SAS, Chemin de I'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Genetically modified Zea mays which have been rendered resistant to attack by the European corn borer (Ostrinia nubilalis and Sesamia nonagrioides) by transgenic expression of a truncated Cry1Ab toxin. Bt11 maize also transgenically expresses the enzyme PAT to achieve tolerance to the herbicide glufosinate ammonium.

2. Bt176 Maize from Syngenta Seeds SAS, Chemin de I'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Genetically modified Zea mays which have been rendered resistant to attack by the European corn borer (Ostrinia nubilalis and Sesamia nonagrioides) by transgenic expression of a Cry1Ab toxin. Bt176 maize also transgenically expresses the enzyme PAT to achieve tolerance to the herbicide glufosinate ammonium.

3. MIR604 Maize from Syngenta Seeds SAS, Chemin de I'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Maize which has been rendered insect-resistant by transgenic expression of a modified Cry3A toxin. This toxin is Cry3A055 modified by insertion of a cathepsin-G-protease recognition sequence. The preparation of such transgenic maize plants is described in WO 03/018810.

4. MON 863 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/DE/02/9. MON 863 expresses a Cry3Bb1 toxin and has resistance to certain Coleoptera insects.

5. IPC 531 Cotton from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/ES/96/02.

6. 1507 Maize from Pioneer Overseas Corporation, Avenue Tedesco, 7 B-1160 Brussels, Belgium, registration number C/NL/00/10. Genetically modified maize for the expression of the protein Cry1F for achieving resistance to certain Lepidoptera insects and of the PAT protein for achieving tolerance to the herbicide glufosinate ammonium.

7. NK603×MON 810 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/GB/02/M3/03. Consists of conventionally bred hybrid maize varieties by crossing the genetically modified varieties NK603 and MON 810. NK603×MON 810 Maize transgenically expresses the protein CP4 EPSPS, obtained from Agrobacterium sp. strain CP4, which imparts tolerance to the herbicide Roundup® (contains glyphosate), and also a Cry1Ab toxin obtained from Bacillus thuringiensis subsp. kurstaki which brings about tolerance to certain Lepidoptera, include the European corn borer.

The term “locus” of a useful plant as used herein is intended to embrace the place on which the useful plants are growing, where the plant propagation materials of the useful plants are sown or where the plant propagation materials of the useful plants will be placed into the soil. An example for such a locus is a field, on which crop plants are growing.

The term “plant propagation material” is understood to denote generative parts of the plant, such as seeds, which can be used for the multiplication of the latter, and vegetative material, such as cuttings or tubers, for example potatoes. There may be mentioned for example seeds (in the strict sense), roots, fruits, tubers, bulbs, rhizomes and parts of plants. Germinated plants and young plants which are to be transplanted after germination or after emergence from the soil, may also be mentioned. These young plants may be protected before transplantation by a total or partial treatment by immersion. Preferably “plant propagation material” is understood to denote seeds.

Components A and B can be used in unmodified form or, preferably, together with carriers and adjuvants conventionally employed in the art of formulation.

To this components A and B and inert carriers are conveniently formulated in known manner to emulsifiable concentrates, coatable pastes, directly sprayable or dilutable solutions, dilute emulsions, wettable powders, soluble powders, dusts, granulates, and also encapsulations e.g. in polymeric substances. As with the type of the compositions, the methods of application, such as spraying, atomizing, dusting, scattering, coating or pouring, are chosen in accordance with the intended objectives and the prevailing circumstances. The compositions may also contain further adjuvants such as stabilizers, antifoams, viscosity regulators, binders or tackifiers as well as fertilizers, micronutrient donors or other formulations for obtaining special effects.

Suitable carriers and adjuvants can be solid or liquid and are substances useful in formulation technology, e.g. natural or regenerated mineral substances, solvents, dispersants, wetting agents, tackifiers, thickeners, binders or fertilizers. Such carriers are for example described in WO 97/33890.

The compositions of the invention can be applied to the locus of the plant or plant to be treated, simultaneously or in succession with further compounds. These further compounds can be e.g. fertilizers or micronutrient donors or other preparations which influence the growth of plants. They can also be herbicides as well as insecticides, fungicides, bactericides, nematicides, molluscicides or mixtures of several of these preparations, if desired together with further carriers, surfactants or application promoting adjuvants customarily employed in the art of formulation. Suitable further compounds are described in WO2008/101682.

A preferred method of the invention is foliar application. The frequency of application and the rate of application will depend on the risk of infestation by the corresponding pathogen. However, the compositions of the invention can also penetrate the plant through the roots via the soil (systemic action) by drenching the locus of the plant with a liquid formulation, or by applying the compounds in solid form to the soil, e.g. in granular form (soil application). In crops of water rice such granulates can be applied to the flooded rice field. The compositions of the invention may also be applied to seeds (coating) by impregnating the seeds or tubers either with a liquid formulation of the fungicide or coating them with a solid formulation.

A formulation, i.e. a composition of the invention and, if desired, comprising a solid or liquid adjuvant, is prepared in a known manner, typically by intimately mixing and/or grinding the compound with extenders, for example solvents, solid carriers and, optionally, surface-active compounds (surfactants).

The agrochemical formulations will usually contain from 0.1 to 99% by weight, preferably from 0.1 to 95% by weight, of the active ingredients, 99.9 to 1% by weight, preferably 99.8 to 5% by weight, of a solid or liquid adjuvant, and from 0 to 25% by weight, preferably from 0.1 to 25% by weight, of a surfactant.

Whereas it is preferred to formulate commercial products as concentrates, the end user will normally use dilute formulations.

Advantageous rates of application are normally from 1 g to 2 kg of active ingredient (a.i.) per hectare (ha), preferably from 10 g to 1 kg a.i./ha, most preferably from 20 g to 600 g a.i./ha. When used as seed drenching agent, convenient rates of application are from 10 mg to 1 g of active substance per kg of seeds. The rate of application for the desired action can be determined by experiments. It depends for example on the type of action, the developmental stage of the useful plant, and on the application (location, timing, application method) and can, owing to these parameters, vary within wide limits.

Said methods are particularly effective against the phytopathogenic organisms of the kingdom Fungi, phylum Basidiomycot, class Uredinomycetes, subclass Urediniomycetidae and the order Uredinales (commonly referred to as rusts). Species of rusts having a particularly large impact on agriculture include those of the family Phakopsoraceae, particularly those of the genus Phakopsora, for example Phakopsora pachyrhizi, which is also referred to as Asian soybean rust, and those of the family Pucciniaceae, particularly those of the genus Puccinia such as Puccinia graminis, also known as stem rust or black rust, which is a problem disease in cereal crops and Puccinia recondita, also known as brown rust.

The compositions of the invention are effective against various microbial species able to cause a microbial infection in an animal. Examples of such microbial species are those causing Aspergillosis such as Aspergillus fumigatus, A. flavus, A. terrus, A. nidulans and A. niger; those causing Blastomycosis such as Blastomyces dermatitidis; those causing Candidiasis such as Candida albicans, C. glabrata, C. tropicalis, C. parapsilosis, C. krusei and C. lusitaniae; those causing Coccidioidomycosis such as Coccidioides immitis; those causing Cryptococcosis such as Cryptococcus neoformans; those causing Histoplasmosis such as Histoplasma capsulatum and those causing Zygomycosis such as Absidia corymbifera, Rhizomucor pusillus and Rhizopus arrhizus. Further examples are Fusarium Spp such as Fusarium oxysporum and Fusarium solani and Scedosporium Spp such as Scedosporium apiospermum and Scedosporium prolificans. Still further examples are Microsporum Spp, Trichophyton Spp, Epidermophyton Spp, Mucor Spp, Sporothorix Spp, Phialophora Spp, Cladosporium Spp, Petriellidium spp, Paracoccidioides Spp and Histoplasma Spp.

The following table provides a selection of compounds of the invention

Cpd No. Structure P.01

P.02

P.03

P.04

P.05

P.06

P.07

P.08

P.09

P.10

P.11

P.12

P.13

P.14

P.15

P.16

P.17

P.18

P.19

P.20

P.21

P.22

P.23

P.24

P.25

P.26

P.27

P.28

P.29

P.30

P.31

P.32

P.33

P.34

P.35

P.36

P.37

P.38

P.39

P.40

P.41

P.42

P.43

P.44

P.45

P.46

P.47

P.48

P.49

P.50

P.51

P.52

P.53

P.54

P.55

P.56

P.57

P.58

P.59

P.60

P.61

P.62

P.63

P.64

P.65

P.66

P.67

P.68

P.69

P.70

P.71

P.72

P.73

P.74

P.75

P.76

P.77

P.78

P.79

P.80

P.81

P.82

P.83

P.84

P.85

P.86

P.87

P.88

P.89

P.90

P.91

P.92

P.93

P.94

P.95

P.96

P.97

P.98

P.99

P.100

P.101

P.101a

P.102

P.103

P.104

P.105

P.106

P.107

P.108

P.109

P.110

P.111

P.112

P.113

P.114

P.115

P.116

P.117

P.118

P.119

P.120

P.121

P.122

P.123

P.124

P.125

P.126

P.127

P.128

P.129

P.130

P.131

P.132

P.133

P.134

P.135

P.136

P.137

P.138

P.139

P.140

P.141

P.142

P.143

P.145

P.146

P.147

P.148

P.149

P.150

P.151

P.152

P.153

P.154

P.155

P.156

P.157

P.158

P.159

P.160

P.161

P.162

P.163

P.164

P.165

P.166

P.167

P.168

P.169

P.170

P.171

P.172

P.173

P.174

P.175

P.176

P.177

P.178

P.179

P.180

P.181

P.182

P.183

P.184

P.185

P.186

P.187

P.188

P.189

P.190

P.191

P.192

P.193

P.194

P.195

P.196

P.197

P.198

P.199

P.200

P.201

P.202

P.203

P.204

P.205

P.206

P.207

P.208

P.209

P.210

P.211

P.212

P.213

P.214

P.215

P.216

P.217

P.218

P.219

P.220

P.221

P.222

P.223

P.224

P.225

P.226

P.227

P.228

P.229

P.230

P.231

P.232

P.233

P.234

P.235

P.236

P.237

P.238

P.239

P.240

P.241

P.242

P.243

P.244

P.245

P.246

P.247

P.248

P.249

P.250

P.251

P.252

P.253

P.254

P.255

P.256

P.257

P.258

P.259

P.260

P.261

P.262

P.263

P.264

P.265

P.266

P.267

P.268

P.269

P.270

P.271

P.272

P.273

P.274

P.275

P.276

P.277

P.278

P.279

P.280

P.281

P.282

P.283

P.284

P.285

P.286

P.287

P.288

P.289

P.290

P.291

P.292

P.293

P.294

P.295

P.296

P.297

P.298

P.299

P.300

P.301

P.302

P.303

P.304

P.305

P.306

P.307

P.308

P.309

P.310

P.311

P.312

P.313

P.314

P.315

P.316

P.317

P.318

P.319

P.320

P.321

P.322

P.323

P.324

P.325

P.326

P.327

P.328

P.329

P.330

P.331

P.332

P.333

P.334

P.335

P.336

P.337

P.338

P.339

P.340

P.341

P.342

P.343

P.344

P.345

P.346

P.347

P.348

P.349

P.350

P.351

P.352

P.353

P.354

P.355

P.356

P.357

P.358

P.359

P.360

P.361

P.362

P.363

P.364

P.365

P.366

P.367

P.368

P.369

P.370

P.371

P.372

Table A discloses 1201 sets of meanings of the variables R₁, R₂, R₅ and R₆ in a compound of formula I.

TABLE A Meanings for R₁, R₂, R₅ and R₆: Line R₁ R₂ R₆ R₅ A.1.1 CH₃ CH₂CH₃ H

A.1.2 CH₃ CH₂CH₃ H

A.1.3 CH₃ CH₂CH₃ H

A.1.4 CH₃ CH₂CH₃ H

A.1.5 CH₃ CH₂CH₃ H

A.1.6 CH₃ CH₂CH₃ H

A.1.7 CH₃ CH₂CH₃ H

A.1.8 CH₃ CH₂CH₃ H

A.1.9 CH₃ CH₂CH₃ H

A.1.10 CH₃ CH₂CH₃ H

A.1.11 CH₃ CH₂CH₃ H

A.1.12 CH₃ CH₂CH₃ H

A.1.13 CH₃ CH₂CH₃ H

A.1.14 CH₃ CH₂CH₃ H

A.1.15 CH₃ CH₂CH₃ H

A.1.16 CH₃ CH₂CH₃ H

A.1.17 CH₃ CH₂CH₃ H

A.1.18 CH₃ CH₂CH₃ H

A.1.19 CH₃ CH₂CH₃ H

A.1.20 CH₃ CH₂CH₃ H

A.1.21 CH₃ CH₂CH₃ H

A.1.22 CH₃ CH₂CH₃ H

A.1.23 CH₃ CH₂CH₃ H

A.1.24 CH₃ CH₂CH₃ H

A.1.25 CH₃ CH₂CH₃ H

A.1.26 CH₃ CH₂CH₃ H

A.1.27 CH₃ CH₂CH₃ H

A.1.28 CH₃ CH₂CH₃ H

A.1.29 CH₃ CH₂CH₃ H

A.1.30 CH₃ CH₂CH₃ H

A.1.31 CH₃ CH₂CH₃ H

A.1.32 CH₃ CH₂CH₃ H

A.1.33 CH₃ CH₂CH₃ H

A.1.34 CH₃ CH₂CH₃ H

A.1.35 CH₃ CH₂CH₃ H

A.1.36 CH₃ CH₂CH₃ H

A.1.37 CH₃ CH₂CH₃ H

A.1.38 CH₃ CH₂CH₃ H

A.1.39 CH₃ CH₂CH₃ H

A.1.40 CH₃ CH₂CH₃ H

A.1.41 CH₃ CH₂CH₃ H

A.1.42 CH₃ CH₂CH₃ H

A.1.43 CH₃ CH₂CH₃ H

A.1.44 CH₃ CH₂CH₃ H

A.1.45 CH₃ CH₂CH₃ H

A.1.46 CH₃ CH₂CH₃ H

A.1.47 CH₃ CH₂CH₃ H

A.1.48 CH₃ CH₂CH₃ H

A.1.49 CH₃ CH₂CH₃ H

A.1.50 CH₃ CH₂CH₃ H

A.1.51 CH₃ CH₂CH₃ H

A.1.52 CH₃ CH₂CH₃ H

A.1.53 CH₃ CH₂CH₃ H

A.1.54 CH₃ CH₂CH₃ H

A.1.55 CH₃ CH₂CH₃ H

A.1.56 CH₃ CH₂CH₃ H

A.1.57 CH₃ CH₂CH₃ H

A.1.58 CH₃ CH₂CH₃ H

A.1.59 CH₃ CH₂CH₃ H

A.1.60 CH₃ CH₂CH₃ H

A.1.61 CH₃ CH₂CH₃ H

A.1.62 CH₃ CH₂CH₃ H

A.1.63 CH₃ CH₂CH₃ H

A.1.64 CH₃ CH₂CH₃ H

A.1.65 CH₃ CH₂CH₃ H

A.1.66 CH₃ CH₂CH₃ H

A.1.67 CH₃ CH₂CH₃ H

A.1.68 CH₃ CH₂CH₃ H

A.1.69 CH₃ CH₂CH₃ H

A.1.70 CH₃ CH₂CH₃ H

A.1.71 CH₃ CH₂CH₃ H

A.1.72 CH₃ CH₂CH₃ H

A.1.73 CH₃ CH₂CH₃ H

A.1.74 CH₃ CH₂CH₃ H

A.1.75 CH₃ CH₂CH₃ H

A.1.76 CH₃ CH₂CH₃ H

A.1.77 CH₃ CH₂CH₃ H

A.1.78 CH₃ CH₂CH₃ H

A.1.79 CH₃ CH₂CH₃ H

A.1.80 CH₃ CH₂CH₃ H

A.1.81 CH₃ CH₂CH₃ H

A.1.82 CH₃ CH₂CH₃ H

A.1.83 CH₃ CH₂CH₃ H

A.1.84 CH₃ CH₂CH₃ H

A.1.85 CH₃ CH₂CH₃ H

A.1.86 CH₃ CH₂CH₃ H

A.1.87 CH₃ CH₂CH₃ H

A.1.88 CH₃ CH₂CH₃ H

A.1.89 CH₃ CH₂CH₃ H

A.1.90 CH₃ CH₂CH₃ H

A.1.91 CH₃ CH₂CH₃ H

A.1.92 CH₃ CH₂CH₃ H

A.1.93 CH₃ CH₂CH₃ H

A.1.94 CH₃ CH₂CH₃ H

A.1.95 CH₃ CH₂CH₃ H

A.1.96 CH₃ CH₂CH₃ H

A.1.97 CH₃ CH₂CH₃ H

A.1.98 CH₃ CH₂CH₃ H

A.1.99 CH₃ CH₂CH₃ H

A.1.100 CH₃ CH₂CH₃ H

A.1.101 CH₃ CH₂CH₃ H

A.1.102 CH₃ CH₂CH₃ H

A.1.103 CH₃ CH₂CH₃ H

A.1.104 CH₃ CH₂CH₃ H

A.1.105 CH₃ CH₂CH₃ H

A.1.106 CH₃ CH₂CH₃ H

A.1.107 CH₃ CH₂CH₃ H

A.1.108 CH₃ CH₂CH₃ H

A.1.109 CH₃ CH₂CH₃ H

A.1.110 CH₃ CH₂CH₃ H

A.1.111 CH₃ CH₂CH₃ H

A.1.112 CH₃ CH₂CH₃ H

A.1.113 CH₃ CH₂CH₃ H

A.1.114 CH₃ CH₂CH₃ H

A.1.115 CH₃ CH₂CH₃ H

A.1.116 CH₃ CH₂CH₃ H

A.1.117 CH₃ CH₂CH₃ H

A.1.118 CH₃ CH₂CH₃ H

A.1.119 CH₃ CH₂CH₃ H

A.1.120 CH₃ CH₂CH₃ H

A.1.121 CH₃ CH₂CH₃ H

A.1.122 CH₃ CH₂CH₃ H

A.1.123 CH₃ CH₂CH₃ H

A.1.124 CH₃ CH₂CH₃ H

A.1.125 CH₃ CH₂CH₃ H

A.1.126 CH₃ CH₂CH₃ H

A.1.127 CH₃ CH₂CH₃ H

A.1.128 CH₃ CH₂CH₃ H

A.1.129 CH₃ CH₂CH₃ H

A.1.130 CH₃ CH₂CH₃ H

A.1.131 CH₃ CH₂CH₃ H

A.1.132 CH₃ CH₂CH₃ H

A.1.133 CH₃ CH₂CH₃ H

A.1.134 CH₃ CH₂CH₃ H

A.1.135 CH₃ CH₂CH₃ H

A.1.136 CH₃ CH₂CH₃ H

A.1.137 CH₃ CH₂CH₃ H

A.1.138 CH₃ CH₂CH₃ H

A.1.139 CH₃ CH₂CH₃ H

A.1.140 CH₃ CH₂CH₃ H

A.1.141 CH₃ CH₂CH₃ H

A.1.142 CH₃ CH₂CH₃ H

A.1.143 CH₃ CH₂CH₃ H

A.1.144 CH₃ CH₂CH₃ H

A.1.145 CH₃ CH₂CH₃ H

A.1.146 CH₃ CH₂CH₃ H

A.1.147 CH₃ CH₂CH₃ H

A.1.148 CH₃ CH₂CH₃ H

A.1.149 CH₃ CH₂CH₃ H

A.1.150 CH₃ CH₂CH₃ H

A.1.151 CH₃ CH₂CH₃ H

A.1.152 CH₃ CH₂CH₃ H

A.1.153 CH₃ CH₂CH₃ H

A.1.154 CH₃ CH₂CH₃ H

A.1.155 CH₃ CH₂CH₃ H

A.1.156 CH₃ CH₂CH₃ H

A.1.157 CH₃ CH₂CH₃ H

A.1.158 CH₃ CH₂CH₃ H

A.1.159 CH₃ CH₂CH₃ H

A.1.160 CH₃ CH₂CH₃ H

A.1.161 CH₃ CH₂CH₃ H

A.1.162 CH₃ CH₂CH₃ H

A.1.163 CH₃ CH₂CH₃ H

A.1.164 CH₃ CH₂CH₃ H

A.1.165 CH₃ CH₂CH₃ H

A.1.166 CH₃ CH₂CH₃ H

A.1.167 CH₃ CH₂CH₃ H

A.1.168 CH₃ CH₂CH₃ H

A.1.169 CH₃ CH₂CH₃ H

A.1.170 CH₃ CH₂CH₃ H

A.1.171 CH₃ CH₂CH₃ H

A.1.172 CH₃ CH₂CH₃ H

A.1.173 CH₃ CH₂CH₃ H

A.1.174 CH₃ CH₂CH₃ H

A.1.175 CH₃ CH₂CH₃ H

A.1.176 CH₃ CH₂CH₃ H

A.1.177 CH₃ CH₂CH₃ H

A.1.178 CH₃ CH₂CH₃ H

A.1.179 CH₃ CH₂CH₃ H

A.1.180 CH₃ CH₂CH₃ H

A.1.181 CH₃ CH₂CH₃ H

A.1.182 CH₃ CH₂CH₃ H

A.1.183 CH₃ CH₂CH₃ H

A.1.184 CH₃ CH₂CH₃ H

A.1.185 CH₃ CH₂CH₃ H

A.1.186 CH₃ CH₂CH₃ H

A.1.187 CH₃ CH₂CH₃ H

A.1.188 CH₃ CH₂CH₃ H

A.1.189 CH₃ CH₂CH₃ H

A.1.190 CH₃ CH₂CH₃ H

A.1.191 CH₃ CH₂CH₃ H

A.1.192 CH₃ CH₂CH₃ H

A.1.193 CH₃ CH₂CH₃ H

A.1.194 CH₃ CH₂CH₃ H

A.1.195 CH₃ CH₂CH₃ H

A.1.196 CH₃ CH₂CH₃ H

A.1.197 CH₃ CH₂CH₃ H

A.1.198 CH₃ CH₂CH₃ H

A.1.199 CH₃ CH₂CH₃ H

A.1.200 CH₃ CH₂CH₃ H

A.1.201 CH₃ CH₂CH₃ H

A.1.202 CH₃ CH₂CH₃ H

A.1.203 CH₃ CH₂CH₃ H

A.1.204 CH₃ CH₂CH₃ H

A.1.205 CH₃ CH₂CH₃ H

A.1.206 CH₃ CH₂CH₃ H

A.1.207 CH₃ CH₂CH₃ H

A.1.208 CH₃ CH₂CH₃ H

A.1.209 CH₃ CH₂CH₃ H

A.1.210 CH₃ CH₂CH₃ H

A.1.211 CH₃ CH₂CH₃ H

A.1.212 CH₃ CH₂CH₃ H

A.1.213 CH₃ CH₂CH₃ H

A.1.214 CH₃ CH₂CH₃ H

A.1.215 CH₃ CH₂CH₃ H

A.1.216 CH₃ CH₂CH₃ H

A.1.217 CH₃ CH₂CH₃ H

A.1.218 CH₃ CH₂CH₃ H

A.1.219 CH₃ CH₂CH₃ H

A.1.220 CH₃ CH₂CH₃ H

A.1.221 CH₃ CH₂CH₃ H

A.1.222 CH₃ CH₂CH₃ H

A.1.223 CH₃ CH₂CH₃ H

A.1.224 CH₃ CH₂CH₃ H

A.1.225 CH₃ CH₂CH₃ H

A.1.226 CH₃ CH₂CH₃ H

A.1.227 CH₃ CH₂CH₃ H

A.1.228 CH₃ CH₂CH₃ H

A.1.229 CH₃ CH₂CH₃ H

A.1.230 CH₃ CH₂CH₃ H

A.1.231 CH₃ CH₂CH₃ H

A.1.232 CH₃ CH₂CH₃ H H— A.1.233 CH₃ CH₂CH₃ H

A.1.234 CH₃ CH₂CH₃ H

A.1.235 CH₃ CH₂CH₃ H

A.1.236 CH₃ CH₂CH₃ H

A.1.237 CH₃ CH₂CH₃ H

A.1.238 CH₃ CH₂CH₃ H

A.1.239 CH₃ CH₂CH₃ H

A.1.240 CH₃ CH₂CH₃ H

A.1.241 CH₃ CH₂CH₃ H

A.1.242 CH₃ CH₂CH₃ H

A.1.243 CH₃ CH₂CH₃ H

A.1.244 CH₃ CH₂CH₃ H

A.1.245 CH₃ CH₂CH₃ H H₃C— A.1.246 CH₃ CH₂CH₃ H

A.1.247 CH₃ CH₂CH₃ H

A.1.248 CH₃ CH₂CH₃ H

A.1.249 CH₃ CH₂CH₃ H

A.1.250 CH₃ CH₂CH₃ H

A.1.251 CH₃ CH₂CH₃ H

A.1.252 CH₃ CH₂CH₃ H

A.1.253 CH₃ CH₂CH₃ H

A.1.254 CH₃ CH₂CH₃ H

A.1.255 CH₃ CH₂CH₃ H

A.1.256 CH₃ CH₂CH₃ H

A.1.257 CH₃ CH₂CH₃ H

A.1.258 CH₃ CH₂CH₃ H

A.1.259 CH₃ CH₂CH₃ H

A.1.260 CH₃ CH₂CH₃ H

A.1.261 CH₃ CH₂CH₃ H

A.1.262 CH₃ CH₂CH₃ H

A.1.263 CH₃ CH₂CH₃ H

A.1.264 CH₃ CH₂CH₃ H

A.1.265 CH₃ CH₂CH₃ H

A.1.266 CH₃ CH₂CH₃ H

A.1.267 CH₃ CH₂CH₃ H

A.1.268 CH₃ CH₂CH₃ H

A.1.269 CH₃ CH₂CH₃ H

A.1.270 CH₃ CH₂CH₃ H

A.1.271 CH₃ CH₂CH₃ H

A.1.272 CH₃ CH₂CH₃ H

A.1.273 CH₃ CH₂CH₃ H

A.1.274 CH₃ CH₂CH₃ H

A.1.275 CH₃ CH₂CH₃ H

A.1.276 CH₃ CH₂CH₃ H

A.1.277 CH₃ CH₂CH₃ H

A.1.278 CH₃ CH₂CH₃ H

A.1.279 CH₃ CH₂CH₃ H

A.1.280 CH₃ CH₂CH₃ H

A.1.281 CH₃ CH₂CH₃ H

A.1.282 CH₃ CH₂CH₃ H

A.1.283 CH₃ CH₂CH₃ H

A.1.284 CH₃ CH₂CH₃ H

A.1.285 CH₃ CH₂CH₃ H

A.1.286 CH₃ CH₂CH₃ H

A.1.287 CH₃ CH₂CH₃ H

A.1.288 CH₃ CH₂CH₃ H

A.1.289 CH₃ CH₂CH₃ H

A.1.290 CH₃ CH₂CH₃ H

A.1.291 CH₃ CH₂CH₃ H

A.1.292 CH₃ CH₂CH₃ H

A.1.293 CH₃ CH₂CH₃ H

A.1.294 CH₃ CH₂CH₃ H

A.1.295 CH₃ CH₂CH₃ H

A.1.296 CH₃ CH₂CH₃ H

A.1.297 CH₃ CH₂CH₃ H

A.1.298 CH₃ CH₂CH₃ H

A.1.299 CH₃ CH₂CH₃ H

A.1.300 CH₃ CH₂CH₃ H

A.1.301 CH₃ CH₂CH₃ H

A.1.302 CH₃ CH₂CH₃ H

A.1.303 CH₃ CH₂CH₃ H

A.1.304 CH₃ CH₂CH₃ H

A.1.305 CH₃ CH₂CH₃ H

A.1.306 CH₃ CH₂CH₃ H

A.1.307 CH₃ CH₂CH₃ H

A.1.308 CH₃ CH₂CH₃ H

A.1.309 CH₃ CH₂CH₃ H

A.1.310 CH₃ CH₂CH₃ H

A.1.311 CH₃ CH₂CH₃ H

A.1.312 CH₃ CH₂CH₃ H

A.1.313 CH₃ CH₂CH₃ H

A.1.314 CH₃ CH₂CH₃ H

A.1.315 CH₃ CH₂CH₃ H

A.1.316 CH₃ CH₂CH₃ H

A.1.317 CH₃ CH₂CH₃ H

A.1.318 CH₃ CH₂CH₃ H

A.1.319 CH₃ CH₂CH₃ H

A.1.320 CH₃ CH₂CH₃ H

A.1.321 CH₃ CH₂CH₃ H

A.1.322 CH₃ CH₂CH₃ H

A.1.323 CH₃ CH₂CH₃ H

A.1.324 CH₃ CH₂CH₃ H

A.1.325 CH₃ CH₂CH₃ H

A.1.326 CH₃ CH₂CH₃ H

A.1.327 CH₃ CH₂CH₃ H

A.1.328 CH₃ CH₂CH₃ H

A.1.329 CH₃ CH₂CH₃ H

A.1.330 CH₃ CH₂CH₃ H

A.1.331 CH₃ CH₂CH₃ H

A.1.332 CH₃ CH₂CH₃ H

A.1.333 CH₃ CH₂CH₃ H

A.1.334 CH₃ CH₂CH₃ H

A.1.335 CH₃ CH₂CH₃ H

A.1.336 CH₃ CH₂CH₃ H

A.1.337 CH₃ CH₂CH₃ H

A.1.338 CH₃ CH₂CH₃ H

A.1.339 CH₃ CH₂CH₃ H

A.1.340 CH₃ CH₂CH₃ H

A.1.341 CH₃ CH₂CH₃ H

A.1.342 CH₃ CH₂CH₃ H

A.1.343 CH₃ CH₂CH₃ H

A.1.344 CH₃ CH₂CH₃ H

A.1.345 CH₃ CH₂CH₃ H

A.1.346 CH₃ CH₂CH₃ H

A.1.347 CH₃ CH₂CH₃ H

A.1.348 CH₃ CH₂CH₃ H

A.1.349 CH₃ CH₂CH₃ H

A.1.350 CH₃ CH₂CH₃ H

A.1.351 CH₃ CH₂CH₃ H

A.1.352 CH₃ CH₂CH₃ H

A.1.353 CH₃ CH₂CH₃ H

A.1.354 CH₃ CH₂CH₃ H

A.1.355 CH₃ CH₂CH₃ H

A.1.356 CH₃ CH₂CH₃ H

A.1.357 CH₃ CH₂CH₃ H

A.1.358 CH₃ CH₂CH₃ H

A.1.359 CH₃ CH₂CH₃ H

A.1.360 CH₃ CH₂CH₃ H

A.1.361 CH₃ CH₂CH₃ H

A.1.362 CH₃ CH₂CH₃ H

A.1.363 CH₃ CH₂CH₃ H

A.1.364 CH₃ CH₂CH₃ H

A.1.365 CH₃ CH₂CH₃ H

A.1.366 CH₃ CH₂CH₃ H

A.1.367 CH₃ CH₂CH₃ H

A.1.368 CH₃ CH₂CH₃ H

A.1.369 CH₃ CH₂CH₃ H

A.1.370 CH₃ CH₂CH₃ H

A.1.371 CH₃ CH₂CH₃ H

A.1.372 CH₃ CH₂CH₃ H

A.1.373 CH₃ CH₂CH₃ H

A.1.374 CH₃ CH₂CH₃ H

A.1.375 CH₃ CH₂CH₃ H

A.1.376 CH₃ CH₂CH₃ H

A.1.377 CH₃ CH₂CH₃ H

A.1.378 CH₃ CH₂CH₃ H

A.1.379 CH₃ CH₂CH₃ H

A.1.380 CH₃ CH₂CH₃ H

A.1.381 CH₃ CH₂CH₃ H

A.1.382 CH₃ CH₂CH₃ H

A.1.383 CH₃ CH₂CH₃ H

A.1.384 CH₃ CH₂CH₃ H

A.1.385 CH₃ CH₂CH₃ H

A.1.386 CH₃ CH₂CH₃ H

A.1.387 CH₃ CH₂CH₃ H

A.1.388 CH₃ CH₂CH₃ H

A.1.389 CH₃ CH₂CH₃ H

A.1.390 CH₃ CH₂CH₃ H

A.1.391 CH₃ CH₂CH₃ H

A.1.392 CH₃ CH₂CH₃ H

A.1.393 CH₃ CH₂CH₃ H

A.1.394 CH₃ CH₂CH₃ H

A.1.395 CH₃ CH₂CH₃ H

A.1.396 CH₃ CH₂CH₃ H

A.1.397 CH₃ CH₂CH₃ H

A.1.398 CH₃ CH₂CH₃ H

A.1.399 CH₃ CH₂CH₃ H

A.1.400 CH₃ CH₂CH₃ H

A.1.401 CH₃ CH₂CH₃ H

A.1.402 CH₃ CH₂CH₃ H

A.1.403 CH₃ CH₂CH₃ H

A.1.404 CH₃ CH₂CH₃ H

A.1.405 CH₃ CH₂CH₃ H

A.1.406 CH₃ CH₂CH₃ H

A.1.407 CH₃ CH₂CH₃ H

A.1.408 CH₃ CH₂CH₃ H

A.1.409 CH₃ CH₂CH₃ H

A.1.410 CH₃ CH₂CH₃ H

A.1.411 CH₃ CH₂CH₃ H

A.1.412 CH₃ CH₂CH₃ H

A.1.413 CH₃ CH₂CH₃ H

A.1.414 CH₃ CH₂CH₃ H

A.1.415 CH₃ CH₂CH₃ H

A.1.416 CH₃ CH₂CH₃ H

A.1.417 CH₃ CH₂CH₃ H

A.1.418 CH₃ CH₂CH₃ H

A.1.419 CH₃ CH₂CH₃ H

A.1.420 CH₃ CH₂CH₃ H

A.1.421 CH₃ CH₂CH₃ H

A.1.422 CH₃ CH₂CH₃ H

A.1.423 CH₃ CH₂CH₃ H

A.1.424 CH₃ CH₂CH₃ H

A.1.425 CH₃ CH₂CH₃ H

A.1.426 CH₃ CH₂CH₃ H

A.1.427 CH₃ CH₂CH₃ H

A.1.428 CH₃ CH₂CH₃ H

A.1.429 CH₃ CH₂CH₃ H

A.1.430 CH₃ CH₂CH₃ H

A.1.431 CH₃ CH₂CH₃ H

A.1.432 CH₃ CH₂CH₃ H

A.1.433 CH₃ CH₂CH₃ H

A.1.434 CH₃ CH₂CH₃ H

A.1.435 CH₃ CH₂CH₃ H

A.1.436 CH₃ CH₂CH₃ H

          Line

          R₅ A.1.437

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H—# A.1.1027

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A.1.1177

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A.1.1190

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A.1.1198

A.1.1199

A.1.1200

A.1.1201

The following tables T1 to T151 disclose preferred compounds of formula I for inclusion as component A in compositions of the invention.

TABLE 1 This table discloses the 1201 compounds T1.1.1 to T1.1.1201 of the formula

(T1) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A. For example, the specific compound T1.1.13 is the compound of the formula T1, in which each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the line A.1.13 of Table A:

(T1.1.13) According to the same system, also all of the other 1201 specific compounds disclosed in the Table 1 as well as all of the specific compounds disclosed in the Tables 2 to T151 are specified analogously.

TABLE 2 This table discloses the 1201 compounds T2.1.1 to T2.1.1201 of the formula

(T2) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 3 This table discloses the 1201 compounds T3.1.1 to T3.1.1201 of the formula

(T3) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 4 This table discloses the 1201 compounds T4.1.1 to T4.1.1201 of the formula

(T4) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 5 This table discloses the 1201 compounds T5.1.1 to T5.1.1201 of the formula

(T5) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 6 This table discloses the 1201 compounds T6.1.1 to T6.1.1201 of the formula

(T6) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 7 This table discloses the 1201 compounds T7.1.1 to T7.1.1201 of the formula

(T7) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 8 This table discloses the 1201 compounds T8.1.1 to T8.1.1201 of the formula

(T8) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 9 This table discloses the 1201 compounds T9.1.1 to T9.1.1201 of the formula

(T9) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 10 This table discloses the 1201 compounds T10.1.1 to T10.1.1201 of the formula

(T10) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 11 This table discloses the 1201 compounds T11.1.1 to T11.1.1201 of the formula

(T11) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 12 This table discloses the 1201 compounds T12.1.1 to T12.1.1201 of the formula

(T12) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 13 This table discloses the 1201 compounds T13.1.1 to T13.1.1201 of the formula

(T13) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 14 This table discloses the 1201 compounds T14.1.1 to T14.1.1201 of the formula

(T14) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 15 This table discloses the 1201 compounds T15.1.1 to T15.1.1201 of the formula

(T15) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 16 This table discloses the 1201 compounds T16.1.1 to T16.1.1201 of the formula (T16)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 17 This table discloses the 1201 compounds T17.1.1 to T17.1.1201 of the formula (T17)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 18 This table discloses the 1201 compounds T18.1.1 to T18.1.1201 of the formula (T18)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 19 This table discloses the 1201 compounds T19.1.1 to T19.1.1201 of the formula (T19)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 20 This table discloses the 1201 compounds T20.1.1 to T20.1.1201 of the formula (T20)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 21 This table discloses the 1201 compounds T21.1.1 to T21.1.1201 of the formula (T21)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 22 This table discloses the 1201 compounds T22.1.1 to T22.1.1201 of the formula (T22)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 23 This table discloses the 1201 compounds T23.1.1 to T23.1.1201 of the formula (T23)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 24 This table discloses the 1201 compounds T24.1.1 to T24.1.1201 of the formula (T24)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 25 This table discloses the 1201 compounds T25.1.1 to T25.1.1201 of the formula (T25)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 26 This table discloses the 1201 compounds T26.1.1 to T26.1.1201 of the formula (T26)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 27 This table discloses the 1201 compounds T27.1.1 to T27.1.1201 of the formula (T27)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 28 This table discloses the 1201 compounds T28.1.1 to T28.1.1201 of the formula (T28)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 29 This table discloses the 1201 compounds T29.1.1 to T29.1.1201 of the formula (T29)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 30 This table discloses the 1201 compounds T30.1.1 to T30.1.1201 of the formula (T30)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 31 This table discloses the 1201 compounds T31.1.1 to T31.1.1201 of the formula (T31)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 32 This table discloses the 1201 compounds T32.1.1 to T32.1.1201 of the formula (T32)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 33 This table discloses the 1201 compounds T33.1.1 to T33.1.1201 of the formula (T33)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 34 This table discloses the 1201 compounds T34.1.1 to T34.1.1201 of the formula (T34)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 35 This table discloses the 1201 compounds T35.1.1 to T35.1.1201 of the formula (T35)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 36 This table discloses the 1201 compounds T36.1.1 to T36.1.1201 of the formula (T36)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 37 This table discloses the 1201 compounds T37.1.1 to T37.1.1201 of the formula (T37)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 38 This table discloses the 1201 compounds T38.1.1 to T38.1.1201 of the formula (T38)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 39 This table discloses the 1201 compounds T39.1.1 to T39.1.1201 of the formula (T39)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 40 This table discloses the 1201 compounds T40.1.1 to T40.1.1201 of the formula (T40)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 41 This table discloses the 1201 compounds T41.1.1 to T41.1.1201 of the formula (T41)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 42 This table discloses the 1201 compounds T42.1.1 to T42.1.1201 of the formula (T42)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 43 This table discloses the 1201 compounds T43.1.1 to T43.1.1201 of the formula (T43)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 44 This table discloses the 1201 compounds T44.1.1 to T44.1.1201 of the formula (T44)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 45 This table discloses the 1201 compounds T45.1.1 to T45.1.1201 of the formula (T45)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 46 This table discloses the 1201 compounds T46.1.1 to T46.1.1201 of the formula (T46)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 47 This table discloses the 1201 compounds T47.1.1 to T47.1.1201 of the formula (T47)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 48 This table discloses the 1201 compounds T48.1.1 to T48.1.1201 of the formula (T48)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 49 This table discloses the 1201 compounds T49.1.1 to T49.1.1201 of the formula (T49)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 50 This table discloses the 1201 compounds T50.1.1 to T50.1.1201 of the formula (T50)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 51 This table discloses the 1201 compounds T51.1.1 to T51.1.1201 of the formula (T51)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 52 This table discloses the 1201 compounds T52.1.1 to T52.1.1201 of the formula (T52)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 53 This table discloses the 1201 compounds T53.1.1 to T53.1.1201 of the formula (T53)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 54 This table discloses the 1201 compounds T54.1.1 to T54.1.1201 of the formula (T54)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 55 This table discloses the 1201 compounds T55.1.1 to T55.1.1201 of the formula (T55)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 56 This table discloses the 1201 compounds T56.1.1 to T56.1.1201 of the formula (T56)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 57 This table discloses the 1201 compounds T57.1.1 to T57.1.1201 of the formula (T57)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 58 This table discloses the 1201 compounds T58.1.1 to T58.1.1201 of the formula (T58)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 59 This table discloses the 1201 compounds T59.1.1 to T59.1.1201 of the formula (T59)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 60 This table discloses the 1201 compounds T60.1.1 to T60.1.1201 of the formula (T60)

in which, for each of these 1201 specific compounds, each of the varia- bles R₁, R₂, R₅ and R₆ has the specific meaning given in the correspond- ing line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 61 This table discloses the 1201 compounds T61.1.1 to T61.1.1201 of the formula (T61)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 62 This table discloses the 1201 compounds T62.1.1 to T62.1.1201 of the formula (T62)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 63 This table discloses the 1201 compounds T63.1.1 to T63.1.1201 of the formula (T63)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 64 This table discloses the 1201 compounds T64.1.1 to T64.1.1201 of the formula (T64)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 65 This table discloses the 1201 compounds T65.1.1 to T65.1.1201 of the formula (T65)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 66 This table discloses the 1201 compounds T66.1.1 to T66.1.1201 of the formula (T66)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 67 This table discloses the 1201 compounds T67.1.1 to T67.1.1201 of the formula (T67)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 68 This table discloses the 1201 compounds T68.1.1 to T68.1.1201 of the formula (T68)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 69 This table discloses the 1201 compounds T69.1.1 to T69.1.1201 of the formula (T69)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 70 This table discloses the 1201 compounds T70.1.1 to T70.1.1201 of the formula (T70)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 71 This table discloses the 1201 compounds T71.1.1 to T71.1.1201 of the formula (T71)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 72 This table discloses the 1201 compounds T72.1.1 to T72.1.1201 of the formula (T72)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 73 This table discloses the 1201 compounds T73.1.1 to T73.1.1201 of the formula (T73)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 74 This table discloses the 1201 compounds T74.1.1 to T74.1.1201 of the formula (T74)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 75 This table discloses the 1201 compounds T75.1.1 to T75.1.1201 of the formula (T75)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 76 This table discloses the 1201 compounds T76.1.1 to T76.1.1201 of the formula (T76)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 77 This table discloses the 1201 compounds T77.1.1 to T77.1.1201 of the formula (T77)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 78 This table discloses the 1201 compounds T78.1.1 to T78.1.1201 of the formula (T78)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 79 This table discloses the 1201 compounds T79.1.1 to T79.1.1201 of the formula (T79)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 80 This table discloses the 1201 compounds T80.1.1 to T80.1.1201 of the formula (T80)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 81 This table discloses the 1201 compounds T81.1.1 to T81.1.1201 of the formula (T81)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 82 This table discloses the 1201 compounds T82.1.1 to T82.1.1201 of the formula (T82)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 83 This table discloses the 1201 compounds T83.1.1 to T83.1.1201 of the formula (T83)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 84 This table discloses the 1201 compounds T84.1.1 to T84.1.1201 of the formula (T84)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 85 This table discloses the 1201 compounds T85.1.1 to T85.1.1201 of the formula (T85)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 86 This table discloses the 1201 compounds T86.1.1 to T86.1.1201 of the formula (T86)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 87 This table discloses the 1201 compounds T87.1.1 to T87.1.1201 of the formula (T87)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 88 This table discloses the 1201 compounds T88.1.1 to T88.1.1201 of the formula (T88)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 89 This table discloses the 1201 compounds T89.1.1 to T89.1.1201 of the formula (T89)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 90 This table discloses the 1201 compounds T90.1.1 to T90.1.1201 of the formula (T90)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 91 This table discloses the 1201 compounds T91.1.1 to T91.1.1201 of the formula

(T91) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 92 This table discloses the 1201 compounds T92.1.1 to T92.1.1201 of the formula

(T92) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 93 This table discloses the 1201 compounds T93.1.1 to T93.1.1201 of the formula

(T93) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 94 This table discloses the 1201 compounds T94.1.1 to T94.1.1201 of the formula

(T94) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 95 This table discloses the 1201 compounds T95.1.1 to T95.1.1201 of the formula

(T95) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 96 This table discloses the 1201 compounds T96.1.1 to T96.1.1201 of the formula

(T96) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 97 This table discloses the 1201 compounds T97.1.1 to T97.1.1201 of the formula

(T97) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 98 This table discloses the 1201 compounds T98.1.1 to T98.1.1201 of the formula

(T98) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 99 This table discloses the 1201 compounds T99.1.1 to T99.1.1201 of the formula

(T99) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 100 This table discloses the 1201 compounds T100.1.1 to T100.1.1201 of the formula

(T100) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 101 This table discloses the 1201 compounds T101.1.1 to T101.1.1201 of the formula

(T101) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 102 This table discloses the 1201 compounds T102.1.1 to T102.1.1201 of the formula

(T102) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 103 This table discloses the 1201 compounds T103.1.1 to T103.1.1201 of the formula

(T103) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 104 This table discloses the 1201 compounds T104.1.1 to T104.1.1201 of the formula

(T104) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 105 This table discloses the 1201 compounds T105.1.1 to T105.1.1201 of the formula

(T105) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 106 This table discloses the 1201 compounds T106.1.1 to T106.1.1201 of the formula

(T106) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 107 This table discloses the 1201 compounds T107.1.1 to T107.1.1201 of the formula

(T107) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 108 This table discloses the 1201 compounds T108.1.1 to T108.1.1201 of the formula

(T108) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 109 This table discloses the 1201 compounds T109.1.1 to T109.1.1201 of the formula

(T109) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 110 This table discloses the 1201 compounds T110.1.1 to T110.1.1201 of the formula

(T110) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 111 This table discloses the 1201 compounds T111.1.1 to T111.1.1201 of the formula

(T111) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 112 This table discloses the 1201 compounds T112.1.1 to T112.1.1201 of the formula

(T112) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 113 This table discloses the 1201 compounds T113.1.1 to T113.1.1201 of the formula

(T113) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 114 This table discloses the 1201 compounds T114.1.1 to T114.1.1201 of the formula

(T114) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 115 This table discloses the 1201 compounds T115.1.1 to T115.1.1201 of the formula

(T115) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 116 This table discloses the 1201 compounds T116.1.1 to T116.1.1201 of the formula

(T116) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 117 This table discloses the 1201 compounds T117.1.1 to T117.1.1201 of the formula

(T117) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 118 This table discloses the 1201 compounds T118.1.1 to T118.1.1201 of the formula

(T118) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 119 This table discloses the 1201 compounds T119.1.1 to T119.1.1201 of the formula

(T119) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 120 This table discloses the 1201 compounds T120.1.1 to T120.1.1201 of the formula

(T120) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 121 This table discloses the 1201 compounds T121.1.1 to T121.1.1201 of the formula

(T121) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 122 This table discloses the 1201 compounds T122.1.1 to T122.1.1201 of the formula

(T122) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 123 This table discloses the 1201 compounds T123.1.1 to T123.1.1201 of the formula

(T123) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 124 This table discloses the 1201 compounds T124.1.1 to T124.1.1201 of the formula

(T124) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 125 This table discloses the 1201 compounds T125.1.1 to T125.1.1201 of the formula

(T125) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 126 This table discloses the 1201 compounds T126.1.1 to T126.1.1201 of the formula

(T126) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 127 This table discloses the 1201 compounds T127.1.1 to T127.1.1201 of the formula

(T127) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 128 This table discloses the 1201 compounds T128.1.1 to T128.1.1201 of the formula

(T128) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 129 This table discloses the 1201 compounds T129.1.1 to T129.1.1201 of the formula

(T129) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 130 This table discloses the 1201 compounds T130.1.1 to T130.1.1201 of the formula

(T130) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 131 This table discloses the 1201 compounds T131.1.1 to T131.1.1201 of the formula

(T131) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 132 This table discloses the 1201 compounds T132.1.1 to T132.1.1201 of the formula

(T132) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 133 This table discloses the 1201 compounds T133.1.1 to T133.1.1201 of the formula

(T133) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 134 This table discloses the 1201 compounds T134.1.1 to T134.1.1201 of the formula

(T134) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 135 This table discloses the 1201 compounds T135.1.1 to T135.1.1201 of the formula

(T135) in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 136 This table discloses the 1201 compounds T136.1.1 to T136.1.1201 of the formula (T136)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 137 This table discloses the 1201 compounds T137.1.1 to T137.1.1201 of the formula (T137)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 138 This table discloses the 1201 compounds T138.1.1 to T138.1.1201 of the formula (T138)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 139 This table discloses the 1201 compounds T139.1.1 to T139.1.1201 of the formula (T139)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 140 This table discloses the 1201 compounds T140.1.1 to T140.1.1201 of the formula (T140)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 141 This table discloses the 1201 compounds T141.1.1 to T141.1.1201 of the formula (T141)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 142 This table discloses the 1201 compounds T142.1.1 to T142.1.1201 of the formula (T142)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 143 This table discloses the 1201 compounds T143.1.1 to T143.1.1201 of the formula (T143)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 144 This table discloses the 1201 compounds T144.1.1 to T144.1.1201 of the formula (T144)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 145 This table discloses the 1201 compounds T145.1.1 to T145.1.1201 of the formula (T145)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 146 This table discloses the 1201 compounds T146.1.1 to T146.1.1201 of the formula (T146)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 147 This table discloses the 1201 compounds T147.1.1 to T147.1.1201 of the formula (T147)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 148 This table discloses the 1201 compounds T148.1.1 to T148.1.1201 of the formula (T148)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 149 This table discloses the 1201 compounds T149.1.1 to T149.1.1201 of the formula (T149)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 150 This table discloses the 1201 compounds T150.1.1 to T150.1.1201 of the formula (T150)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 151 This table discloses the 1201 compounds T151.1.1 to T151.1.1201 of the formula (T151)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 152 This table discloses the 1201 compounds T152.1.1 to T152.1.1201 of the formula (T152)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the coresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 153 This table discloses the 1201 compounds T153.1.1 to T153.1.1201 of the formula (T153)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 154 This table discloses the 1201 compounds T154.1.1 to T154.1.1201 of the formula (T154)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 155 This table discloses the 1201 compounds T155.1.1 to T155.1.1201 of the formula (T155)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 156 This table discloses the 1201 compounds T156.1.1 to T156.1.1201 of the formula (T156)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 157 This table discloses the 1201 compounds T157.1.1 to T157.1.1201 of the formula (T157)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 158 This table discloses the 1201 compounds T158.1.1 to T158.1.1201 of the formula (T158)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 159 This table discloses the 1201 compounds T159.1.1 to T159.1.1201 of the formula (T159)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 160 This table discloses the 1201 compounds T160.1.1 to T160.1.1201 of the formula (T160)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 161 This table discloses the 1201 compounds T161.1.1 to T161.1.1201 of the formula (T161)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 162 This table discloses the 1201 compounds T162.1.1 to T162.1.1201 of the formula (T162)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 163 This table discloses the 1201 compounds T163.1.1 to T163.1.1201 of the formula (T163)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1.1 to A.1.1201 of Table A.

TABLE 164 This table discloses the 1201 compounds T164.1.1 to T164.1.1201 of the formula (T164)

in which, for each of these 1201 specific compounds, each of the variables R₁, R₂, R₅ and R₆ has the specific meaning given in the corresponding line, appropriately selected from the 1201 lines A.1. to A.1.1201 of Table A.

In further embodiments the invention provides novel intermediates to provide compounds according to formula (I) are compounds of formula (IV)

wherein R₁₀₀ is wherein R₁₀₀ is halogen, SH, C₁-C₄-alkylthio, C₁-C₄-alkysulfinyl, C₁-C₄-alkylsulfonyl and R₁, R₂, R₃, R₄, R₆ and R₇ are as described herein for compounds of formula (I).

The following table provides a selection of compounds of formula (IV)

R.01

R.02

Mp: 168- 170° C. R.03

R.04

R.05

R.06

R.07

R.08

R.09

R.10

R.11

R.12

Mp: 85-87° C. R.13

R.14

R.15

R.16

R.17

R.18

R.19

R.20

R.21

R.22

Oil; (M + 1)⁺ 300 R.23

R.24

R.25

R.26

R.27

R.28

R.29

R.30

R.31

R.32

Oil; (M + 1)⁺ 290 R.33

R.34

R.35

R.36

R.37

R.38

R.39

R.40

R.41

R.42

R.43

R.44

R.45

R.46

R.47

R.48

R.49

R.50

R.51

R.52

R.53

R.54

R.55

R.56

R.57

R.58

R.59

R.60

The active compounds of component B are known e.g. from the Pesticide Manual (British Crop Protection Council). N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide has the Chemical Abstracts Registry Number [1072957-71-1]. The compound of formula (II) has the Chemical Abstracts Registry Number [173662-97-0]. The compounds (S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol, 3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol are found in WO2010069881.

The active ingredient mixture of the compounds of formula I selected from tables T1 to T164 or a specific compound selected from P.1 to P.372 with active ingredients described above comprises a compound selected from tables T1 to T164 and an active ingredient as described above preferably in a mixing ratio of from 100:1 to 1:6000, especially from 50:1 to 1:500, more especially in a ratio of from 20:1 to 1:200, even more especially from 10:1 to 1:100, very especially from 5:1 and 1:50, special preference being given to a ratio of from 3:1 to 1:10, and a ratio of from 3:1 to 1:5 being likewise preferred, above all in a ratio of 1:1, or 5:1, or 5:2, or 5:3, or 5:4, or 4:1, or 4:2, or 4:3, or 3:1, or 3:2, or 2:1, or 1:5, or 2:5, or 3:5, or 4:5, or 1:4, or 2:4, or 3:4, or 1:3, or 2:3, or 1:2, or 1:600, or 1:300, or 1:150, or 1:35, or 2:35, or 4:35, or 1:75, or 2:75, or 4:75, or 1:6000, or 1:3000, or 1:1500, or 1:350, or 2:350, or 4:350, or 1:750, or 2:750, or 4:750. Those mixing ratios are understood to include, on the one hand, ratios by weight and also, on other hand, molar ratios.

The mixtures comprising a compound of formula I e.g. selected from tables T1 to T164 or a specific compound selected from P.1 to P.372 and one or more active ingredients as described above can be applied, for example, in a single “ready-mix” form, in a combined spray mixture composed from separate formulations of the single active ingredient components, such as a “tank-mix”, and in a combined use of the single active ingredients when applied in a sequential manner, i.e. one after the other with a reasonably short period, such as a few hours or days. The order of applying the compounds of formula I e.g. those selected from tables T1 to T164 and the active ingredients as described above is not essential for working the present invention.

A synergistic effect exists whenever the action of an active ingredient combination is greater than the sum of the actions of the individual components.

The action to be expected E for a given active ingredient combination obeys the so-called COLBY formula and can be calculated as follows (COLBY, S. R. “Calculating synergistic and antagonistic responses of herbicide combination”. Weeds, Vol. 15, pages 20-22; 1967):

ppm=milligrams of active ingredient (=a.i.) per liter of spray mixture

X=% action by active ingredient A) using p ppm of active ingredient

Y=% action by active ingredient B) using q ppm of active ingredient.

According to COLBY, the expected (additive) action of active ingredients A)+B) using p+q ppm of active ingredient is

$E = {X + Y - \frac{X \cdot Y}{100}}$

If the action actually observed (O) is greater than the expected action (E), then the action of the combination is super-additive, i.e. there is a synergistic effect. In mathematical terms the synergism factor SF corresponds to O/E. In the agricultural practice an SF of ≧1.2 indicates significant improvement over the purely complementary addition of activities (expected activity), while an SF of ≦0.9 in the practical application routine signals a loss of activity compared to the expected activity.

EXAMPLES Preparation of 1-(3,5-difluorophenyl)ethanol

To a colorless stirred solution of ^(3′,5′)-difluoroacetophenone (50.00 g, 320.24 mmol) in methanol (320 mL), sodium borohydride (3.41 g, 86.47 mmol, 0.27 eq) was added portion wise over 20 minutes at room temperature under inert atmosphere (Ar). Then the reaction mixture was stirred for 45 min at room temperature and then quenched carefully by the addition of a saturated aqueous ammonium chloride solution (150 mL). The extraction was carried out with ethyl acetate (2×200 mL). The combined organic layers were washed with brine (200 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give the title compound (50.29 g, 99%) as a colorless oil. The alcohol was used as such in the subsequent step.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.27.

Preparation of (−)-(S)-1-(3,5-difluorophenyl)ethanol

To a stirred solution of (−)-DIP-Cl ((—)-diisopinocampheylboron chloride) (2.67 g, 8.33 mmol, 1.3 eq) in THF (20 mL) kept under inert atmosphere (Ar) and cooled to −27° C. to −25° C., ^(3′,5′)-difluoroacetophenone (1.00 g, 6.40 mmol) was added drop wise over 2 min. The reaction was maintained at this temperature for 17 h. The reaction mixture was then treated with acetaldehyde (0.44 mL, 7.69 mmol, 1.2 eq). Thereafter, the temperature was allowed to reach room temperature and the reaction mixture was stirred at for 7 h. The solvent was then removed in vacuo and the resulting residue was partitioned between water (10 mL) and TBME (tert-butyl-methyl ether) (20 mL). The aqueous phase was extracted again with TBME (20 mL). The organic layer was washed with an aqueous 2 N NaOH solution (20 mL), brine (20 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a residue, which was purified by two subsequent column chromatographic steps: First by normal phase chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-9/1) followed by a reversed phase chromatography (90 C₁₈-silica gel, acetonitrile for the second one). This gave the title compound (0.40 g, 40%) as a colorless oil with a specific rotation of [α]²⁵ _(D)=−26.66 (c=1.054 g/100 mL, CH₂Cl₂, 589 nm).

Preparation of cis and trans 4-isopropylcyclohexanol

To a stirred solution of 4-isopropylcyclohexanone (10.00 g, 68.46 mmol) in tert-butyl methyl ether (136 mL) cooled to 7° C. (cooling bath with a cyclohexane/liquid nitrogen slurry), a 1.00 M solution of lithium aluminium hydride in THF (23 mL, 22.59 mmol, 0.33 eq) was added drop wise over 35 minutes while keeping the temperature in the range of 7 to 10° C. Stirring was continued under these conditions. The reaction mixture was then allowed to reach room temperature and stirred at this temperature for an additional 40 minutes. It was then carefully quenched by the slow addition of water (20 mL), followed by a one molar aqueous sulfuric acid solution (60 mL). The extraction was carried out with tert-butyl methyl ether (2×50 mL). The organic layer was washed with a saturated aqueous Na₂CO₃ solution (80 mL), brine (80 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a residue, which was purified by column chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-9/1). Fractions containing the pure compounds were collected and concentrated in vacuo to give pure trans (6.91 g, 71%) and the pure cis isomer (0.68 g, 5%) of 4-isopropyl-cyclohexanol both as colourless oils.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, detection by spraying with Mo—Ce reagent, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of cis 4-isopropylcyclohexanol=0.20); R_(f) of trans 4-isopropylcyclohexanol=0.15.

Preparation of 3-bromo-2-(cis-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine

To a stirred suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (23.65 g, 101.5 mmol) in THF (180 mL), trans isopropylcyclohexanol (14.44 g, 101.5 mmol, 1.0 eq) and triphenylphosphine (32.27 g, 121.8 mmol, 1.2 eq) were added at room temperature under inert atmosphere (Ar). To this mixture, DIAD (diisopropyl diazodicarboxylate) (25.51 mL, 121.8 mmol, 1.2 eq) was added drop wise over 45 min while keeping the temperature below 45° C. Then, the reaction mixture was stirred for 5 h under heating to reflux. TLC indicated that the starting material was consumed. The reaction mixture was therefore allowed to reach room temperature and it was quenched by the addition of water (250 mL). The extraction was carried out with ethyl acetate (3×200 mL). The organic layer was washed with brine (300 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a residue, which was purified by column chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-98/2). Fractions containing the pure compound were collected and concentrated in vacuo to give title compound (22.59 g, 62%) in the form of an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.64.

Preparation of 5-bromo-6-(cis-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine

To a stirred solution of 3-bromo-2-(cis-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine (22.59 g, 63.24 mmol) in EtOH/H₂O (600 mL/150 mL, 4/1 v/v), ammonium chloride (3.45 g, 63.24 mmol, 1.0 eq) and iron powder (14.27 g, 253.0 mmol, 4 eq) were added at room temperature under inert atmosphere (Ar). The reaction mixture was stirred for 3 h under heating to reflux. As TLC indicated that the starting material was consumed at this point in time, the reaction mixture was cooled to room temperature and filtered through a pad of celite. The resulting filtrate was concentrated in vacuo and the residue partitioned between a 2 molar aqueous NaOH solution (100 mL) and ethyl acetate (150 mL). After phase separation, the aqueous phase was extracted once more with ethyl acetate (2×100 mL). The organic layer was washed with brine (400 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to afford the title compound (21.01 g, 101%) in the form of an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.19.

Preparation of N′-[5-bromo-6-(cis-4-isopropylcyclohexoxy)-2-methyl-3-pyridyl]-N-ethyl-N-methyl formamidine

The Vilsmeier reagent was freshly prepared by the slow addition of phosphorus oxychloride (7.09 mL, 75.89 mmol, 1.2 eq) to a solution of N,N-ethylmethylformamide (6.61 g, 75.89 mmol, 1.2 eq) in dichloromethane (75 mL) at room temperature. After the addition was complete, he reaction mixture was stirred at room temperature for 1 h. The Vilsmeier reagent was then added drop wise over 40 min to a solution of 5-bromo-6-(cis-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine (20.70 g, 63.24 mmol) in dichloromethane (225 mL) at room temperature under inert atmosphere (Ar). Stirring was continued for 1.5 h at room temperature. The reaction mixture was then quenched by the addition of water (100 mL) and the pH was adjusted to 14 by the addition of a 2.0 molar aqueous NaOH solution (80 mL). The phases were separated and the aqueous phase extracted with dichloromethane (2×100 mL). The organic layer was washed with brine (250 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a residue, which was purified by column chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-4/1). Fractions containing the pure compound were collected and concentrated in vacuo to give the title compound (20.23 g, 81%) as a yellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.29.

¹H NMR (400 MHz, CDCl₃): δ (ppm)=7.45-7.30 (broad s, 1H), 7.23 (s, 1H), 5.32-5.28 (m, 1H), 3.55-3.24 (broad s, 2H), 2.98 (s, 3H), 2.35 (s, 3H), 2.04-2.01 (m, 2H), 1.63-1.46 (m, 7H), 1.20 (t, 3H), 1.18-1.10 (m, 1H), 0.91-0.89 (d, 6H).

Preparation of 3-bromo-2-(trans-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine

To a stirred suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (2.00 g, 8.58 mmol) in THF (8.6 mL), cis isopropylcyclohexanol (1.44 g, 8.58 mmol, 1.0 eq) and triphenylphosphine (2.73 g, 10.30 mmol, 1.2 eq) were added at room temperature under inert atmosphere (Ar). To this mixture, DIAD (diisopropyl diazodicarboxylate) (2.16 mL, 10.30 mmol, 1.2 eq) was added drop wise over 10 minutes while keeping the temperature below 40° C. The reaction mixture was stirred for 1.5 h under heating to. After this point in time, TLC indicted consumption of the starting material and the reaction mixture was allowed to reach room temperature and was quenched by adding water (20 mL). The water phase was extracted with ethyl acetate (3×20 mL). The organic layer was washed with brine (35 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a residue, which was purified by column chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-9/1). Fractions containing the pure compound were collected and concentrated in vacuo to give the title compound (0.94 g, 30%) as an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.65.

Preparation of 5-bromo-6-(trans-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine

To a stirred solution of 3-bromo-2-(trans-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine (0.917 g, 2.00 mmol) in EtOH/H₂O (24 mL/6 mL, 4/1 v/v), ammonium chloride (0.109 g, 2.00 mmol, 1.0 eq) and iron powder (0.452 g, 8.00 mmol, 4 eq) were added at room temperature under inert atmosphere (Ar). The reaction mixture was stirred under heating to reflux for 3 h. At this point in time, TLC indicated that the starting material was consumed. Therefore, the reaction mixture was allowed to reach room temperature and was filtered through a pad of celite. The filtrate was concentrated under reduced pressure and the residue partitioned between a 2 molar aqueous NaOH solution (20 mL) and ethyl acetate (30 mL). The phases were separated and the aqueous phase extracted with ethyl acetate (2×20 mL). The organic layer was washed with brine (40 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to afford the title compound (0.658 g, 100%) as an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.19.

Preparation of 5-bromo-6-(trans-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine

The Vilsmeier reagent was freshly prepared by the slow addition of phosphorus oxychloride (0.101 mL, 1.08 mmol, 1.2 eq) to a solution of N,N-ethylmethylformamide (0.094 g, 1.08 mmol, 1.2 eq) in dichloromethane (0.5 mL) at room temperature. After the addition was complete, the reaction mixture was stirred at room temperature for 1 h. Then the Vilsmeier reagent thus obtained was added drop wise to a solution of 5-bromo-6-(trans-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine (0.295 g, 0.90 mmol) in dichloromethane (1.0 mL) at room temperature under inert atmosphere (Ar). Stirring was continued was for 1.5 h at room temperature. The reaction was then quenched by the addition of a 2 molar aqueous NaOH solution (5 mL). The phases were separated and the aqueous phase extracted with dichlormethane (2×10 mL). The organic layer was washed with brine (10 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a residue, which was purified by column chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-4/1). Fractions containing the pure compound were collected and concentrated in vacuo to give the title compound (0.191 g, 54%) as a light yellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.29.

¹H NMR (400 MHz, CDCl₃): δ (ppm)=7.45-7.30 (broad s, 1H), 7.22 (s, 1H), 4.93-4.85 (m, 1H), 3.55-3.22 (broad s, 2H), 2.98 (s, 3H), 2.35 (s, 3H), 2.19-2.15 (m, 2H), 1.80-1.77 (m, 2H), 1.50-1.09 (m, 5H), 1.28 (t, 3H), 0.88-0.86 (d, 6H).

Preparation of N-Ethyl-N-methyl-formamide

113 g (1.912 mol) of ethylmethylamine was dissolved in 500 mL of dry toluene. 75.86 mL of formic acid (92.2 g, 2.01 mol) was added drop-wise over 20 minutes. Hereby, an exothermic reaction was observed. The temperature was kept below 35° C. by cooling with an ice-water cooling bath. The turbid solution was stirred under heating to reflux (bath temperature of 175° C.) and the water removed using a Dean and Stark separator. 46 mL of water phase was thus separated. This water phase was extracted with 50 mL of ethyl acetate. And this ethyl acetate solution was added to the reaction mixture, after this one was allowed to reach room temperature. After evaporation of the solvent, the resulting liquid was subjected to a fractionating column distillation (Widmer column) at 80 mbar. 138 g of a colourless liquid of bp=95-96° C. was collected. As this material was contaminated with formic acid, the liquid was taken up in 1.0 L of ethyl acetate and kept over K₂CO₃ (occasional stirring, 24 h overall). The solution was then filtered and washed with water and the organic phase was again subjected to the distillation procedure mentioned before. This gave 130.4 g of the title compound as a liquid (bp=95-96° C., 80 mbar).

Preparation of methoxyethylmethyl-methanaminium methyl sulfate

128 g of N-ethyl-N-methyl-formamide was added slowly to 139 mL (185 g, 1.469 mol) of dimethyl sulfate (the dimethyl sulfate used was freshly distilled in vacuo after having been tried over K₂CO₃). The colourless solution was warmed under stirring to 50° C. whereupon an exothermic reaction was starting up. The heating bath was removed and the reaction mixture reached a temperature of 86° C. After the exothermicity came to an end, the reaction mixture was stirred at a temperature of 80° C. for an additional 3 hours. Thereafter, the reaction mixture was allowed to reach room temperature. The resulting liquid was then shaken in a separatory funnel first with 100 mL of toluene and, after phase separation, with 100 mL of diethyl ether. Traces of solvents were removed in vacuo (rotovapor) to give 294 g of the title compound in the form of a colourless liquid. The compound was used as such in the subsequent step.

Preparation of 5-Bromo-2-methyl-3-nitro-6-[2,2,2-trifluoro-1-(4-fluorophenyl)ethoxy]pyridine

To a stirred suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (0.10 g, 0.43 mmol) in THF (3 mL), 2,2,2-trifluoro-1-(4-fluorophenyl)ethanol (0.13 g, 0.64 mmol, 1.5 equiv) and triphenylphosphine (0.17 g, 0.64 mmol, 1.5 eq) were added at room temperature under inert atmosphere (Ar). To this mixture, DIAD (diisopropyl diazodicarboxylate) (0.13 mL, 0.64 mmol, 1.5 eq) was added dropwise over 10 minutes while keeping the temperature below 40° C. The reaction mixture was stirred for 6 h under heating at 60° C. After this time, TLC indicted that the starting material had been consumed and the reaction mixture was allowed to reach room temperature before quenching with water (10 mL). The water phase was extracted with ethyl acetate (3×15 mL). The organic layer was washed with brine (20 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a brown residue, which was purified by combiflash column chromatography (silica gel, heptane/ethyl acetate, v/v=95/5). Fractions containing the pure compound were collected and concentrated in vacuo to give the title compound (0.11 g, 62% yield) as a yellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v); R_(f) of the title compound=0.65.

Preparation of 2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol

In a 50 mL two-neck flask, 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanone (2.0 g, 8.3 mmol) was dissolved in methanol (8 mL) and sodium borohydride (0.31 g, 8.3 mmol) was added carefully in portions with ice-bath cooling. The resultant colourless solution was stirred at RT for 2 hours and monitored by TLC. Upon the disappearance of all starting material, 5 mL of an aqueous saturated NH₄Cl solution was slowly added to the reaction mixture with additional stirring for 10 min. The later was extracted 3 times with 20 mL of EtOAc and the organic fractions were combined and washed with 10 mL of brine, dried over Na₂SO₄, and filtered. The solvent was removed under reduced pressure to give 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol (2.13 g, quantitative) as a colourless oil which was used with no further purification.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 2:1 (v/v); R_(f) of the title compound=0.50.

Preparation of 5-Bromo-2-methyl-3-nitro-6-[2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethoxyl]pyridine

To a stirring suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (0.25 g, 1.07 mmol) in THF (7 mL), 2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol (0.39 g, 1.61 mmol, 1.5 equiv) and triphenylphosphine (0.42 g, 1.61 mmol, 1.5 eq) were added at room temperature under inert atmosphere (Ar). To this mixture, DIAD (diisopropyl diazodicarboxylate) (0.33 mL, 1.61 mmol, 1.5 eq) was added dropwise over 10 minutes while keeping the temperature below 40° C. The reaction mixture was stirred for 6 h under heating at 60° C. After this time, TLC indicted that the starting material was consumed and the reaction mixture was allowed to reach room temperature before quenching with water (10 mL). The water phase was extracted with ethyl acetate (2×50 mL). The organic layer was washed with brine (20 mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to give a brown residue, which was purified by combiflash column chromatography (silica gel, heptane/ethyl acetate, v/v=95/5). Fractions containing the pure compound were collected and concentrated in vacuo to give the title compound (0.18 g, 41% yield) as a yellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere in developing tank, UV detection, eluent: heptanes/ethyl acetate 2:1 (v/v); R_(f) of the title compound=0.74.

Preparation of 1,1,1-Trifluorohept-6-en-2-ol

To a ice-bath cooled solution of hex-5-enal (500 mg, 4.331 mmol) and trimethyl(trifluoromethyl)silane (0.74 g, 5.13 mmol, 1.2 equiv.) in THF (10 mL) was added tetrabutylammonium hydrofluoride (10 mg, 0.04 mmol). The ice bath was removed and the reaction progress was monitored via GCMS and 1H NMR. Upon complete transformation of the starting material the reaction mixture was treated with 2M HCl and stirred for an additional 2 h. Then, 50 mL of Et₂O was introduced and the layers were separated. The aqueous fraction was additionally extracted with Et₂O and the combined organic phases were washed sequentially with a saturated aqueous NaHCO₃ solution, water, and brine. After drying with MgSO₄ and filtration the solvent was removed under reduced pressure and the resultant crude residue was purified by column chromatography (silica gel, pentane/Et₂O, v/v=8/2). Fractions containing the pure compound were collected and concentrated in vacuo to give 1,1,1-trifluorohept-6-en-2-ol (225 mg, 31% yield) as a yellow oil.

Using techniques analogous to those above and further techniques known to the person skilled in the art, for example as found in WO 08/101682, the compounds found in Table Q were prepared.

TABLE Q LC-Method: R_(t) (min); MS-ESI (m/z; (M + H)⁺) Q.001

Method 4: 1.42 min; 370 Q.002

Method 4: 1.46 min; 358 Q.003

Method 4: 1.30 min; 328 Q.004

Method 4: 1.33 min; 342 Q.005

Method 4: 1.17 min; 398 Q.006

Gum Q.007

Method 4: 1.32 min; 292 Q.008

Method 4: 1.39 min; 356 Q.009

Mp 72-73° C. Q.010

Method 4: 1.42 min; 356 Q.011

Gum Q.012

Gum Q.013

Gum Q.014

Gum Q.015

Gum Q.016

Gum Q.017

Gum Q.018

Gum Q.019

Gum Q.020

Gum Q.021

Gum Q.022

Gum Q.023

Gum Q.024

Gum Q.025

Gum Q.026

Gum Q.027

Gum Q.028

Method 4: 1.32 min; 418 Q.029

Liquid Q.030

Method 4: 1.53 min; 544 Q.031

Gum Q.032

Liquid Q.033

Method 4: 1.31 min; 444 Q.034

Method 4: 1.22 min; 340 Q.035

Method 4: 0.99 min; 358 Q.036

Method 4: 0.98 min; 388 Q.037

Solid Q.038

Liquid Q.039

Method 4: 1.48 min; 473 Q.040

Liquid Q.041

Liquid Q.042

Liquid Q.043

Liquid Q.044

Method 4: 1.28 min; 446 Q.045

Gum Q.046

Gum Q.047

Gum Q.048

Gum Q.049

Gum Q.050

Gum Q.051

Liquid Q.052

Method 4: 1.18 min; 360 Q.053

Liquid Q.054

Liquid Q.055

Liquid Q.056

Solid Q.057

Method 4: 1.19 min; 276 Q.058

Method 4: 1.64 min; 348 Q.059

Method 4: 1.00 min; 392 Q.060

Method 4: 1.16 min; 420 Q.061

Liquid Q.062

Method 4: 1.34 min; 388 Q.063

Method 4: 1.16 min; 338 Q.064

Mp 77-78° C. Q.065

Liquid Q.066

Liquid Q.067

Liquid Q.068

Solid Q.069

Method 4: 1.30 min; 410 Q.070

Liquid Q.071

Gum Q.072

Solid Q.073

Solid Q.074

Liquid Q.075

Liquid Q.076

Liquid Q.077

Liquid Q.078

Liquid Q.079

Method 4: 1.39 min; 368 Q.080

Liquid Q.081

Liquid Q.082

Liquid Q.083

Liquid Q.084

Liquid Q.085

Gum Q.086

Liquid Q.087

Liquid Q.088

Liquid Q.089

Liquid Q.090

Liquid Q.091

Liquid Q.092

Liquid Q.093

Gum Q.094

Liquid Q.095

Method 1: 13.577 min; 362 Q.096

Mp 81-82° C. Q.097

Method 2: 11.956 min; 398 Q.098

Method 1: 11.773 min; 352 Q.099

Method 1: 11.755 min; 376 Q.100

Method 1: 12.320 min; 390 Q.101

Method 1: 12.207 min; 440 Q.102

Method 1: 11.873 min; 376 Q.103

Method 1: 13.153 min; 382 Q.104

Method 1: 6.418 min; 438 Q.105

Method 1: 11.571 min; 400 Q.106

Method 1: 12.115 min; 365 Q.107

Mp 107-108° C. Q.108

Method 2: 12.713 min; 523 Q.109

Method 1: 12.881 min; 479 Q.110

Method 2: 12.214 min; 402 Q.111

Mp 57-59° C. Q.112

Method 2: 12.236 min; 390 Q.113

Method 1: 12.030 min; 412 Q.114

Method 2: 13.002 min; 404 Q.115

Method 1: 9.589 min; 393 Q.116

Method 2: 11.625 min; 394 Q.117

Method 2: 6.956 min; 377 Q.118

Method 2: 12.577 min; 368 Q.119

Method 1: 13.850 min; 444 Q.120

Method 2: 11.861 min; 354 Q.121

Method 2: 12.977 min; 451 Q.122

Method 2: 13.353 min; 394 Q.123

Mp 120-121° C. Q.124

Mp 98-99° C. Q.125

Mp 101-102° C. Q.126

Method 1: 13.029 min; 480 Q.127

Method 2: 13.168 min; 481 Q.128

Mp 60-62° C. Q.129

Mp 46-48° C. Q.130

Method 2: 3.41 min; 377 Q.131

Method 2: 12.242 min; 408 Q.132

Method 1: 12.688 min; 368 Q.133

Method 1: 12.522 min; 368 Q.134

Method 2: 12.979 min; 380 Q.135

Method 3: 1.49 min; 396: Cis Q.136

Method 1: 10.914 min; 431 Q.137

Mp 43-45° C. Q.138

Method 1: 13.065 min; 402 Q.139

Method 1: 13.387 min; 370 Q.140

Method 2: 12.176 min; 366 Q.141

Method 1: 12.712 min; 368 Q.142

Method 1: 13.557 min; 466 Q.143

Mp 71-73° C. Q.144

Method 1: 11.879 min; 503 Q.145

Mp 106-107° C. Q.146

Method 1: 11.862 min; 344 Q.147

Method 1: 12.605 min; 404 Q.148

Method 1: 12.704 min; 405 Q.149

Method 1: 12.642 min; 370 Q.150

Method 1: 13.317 min; 372 Q.151

Liquid Q.152

Mp 100-101° C. Q.153

Mp 43-44° C. Q.154

Mp 53-57° C. Q.155

Mp 75-78° C. Q.156

Mp 90-91° C. Q.157

Mp 125-127° C. Q.158

Liquid Q.159

Liquid Q.160

Liquid Q.161

Liquid Q.162

Liquid Q.163

Mp 90-95° C. Q.164

Mp 88-89° C. Q.165

Liquid Q.166

Liquid Q.167

Liquid Q.168

Liquid Q.169

Liquid Q.170

Liquid Q.171

Liquid Q.172

Mp 72-76° C. Q.173

Liquid Q.174

Liquid Q.175

Liquid Q.176

Liquid Q.177

Liquid Q.178

Method 2: 12.011 min; 460 Q.179

Method 1: 13.777 min; 444; Trans Q.180

Method 1: 13.653 min; 444; Cis Q.181

Method 2: 11.260 min; 334 Q.182

Method 1: 13.163 min; 318; Trans Q.183

Method 1: 14.926 min; 318; Cis Q.184

Method 2: 12.116 min; 348 Q.185

Method 1: 14.256 min; 332; Trans Q.186

Method 1: 15.845 min; 332; Cis Q.187

Method 2: 12.707 min; 426 Q.188

Method 2: 12.145 min; 426 Q.189

Method 2: 11.943 min; 422 Q.190

Method 1: 12.216 min; 436 Q.191

Method 2: 12.769 min; 426 Q.192

Method 2: 12.121 min; 424 Q.193

Method 2: 11.891 min; 424 Q.194

Method 2: 11.881 min; 422 Q.195

Mp 52-54° C. Q.196

Method 1: 12.439 min; 466 Q.197

Method 1: 11.886 min; 416 Q.198

Method 1: 11.886 min; 390 Q.199

Method 1: 11.955 min; 418 Q.200

Method 1: 12.096 min; 402 Q.201

Method 1: 12.796 min; 418 Q.202

Method 1: 12.154 min; 496 Q.203

Method 2: 13.148 min; 404 Q.204

Method 2: 11.780 min; 412 Q.205

Method 1: 6.785 min; 444 Q.206

Mp 75-78° C. Q.207

Mp 57-58° C. Q.208

Method 1: 10.753 min; 368 Q.209

Method 1: 7.472 min; 413 Q.210

Mp 134-135° C. Q.211

Method 1: 11.913 min; 440 Q.212

Method 1: 11.392 min; 410 Q.213

Method 1: 8.301 min; 370 Q.214

Method 1: 11.318 min; 364 Q.215

Method 1: 12.017 min; 384 Q.216

Method 2: 12.660 min; 374 Q.217

Method 1: 12.015 min; 426 Q.218

Method 2: 12.403 min; 408 Q.219

Method 2: 13.469 min; 418 Q.220

Method 1: 11.837 min; 354 Q.221

Method 1: 13.221 min; 458 Q.222

Method 2: 11.427 min; 340 Q.223

Method 1: 12.006 min; 390 Q.224

Method 2: 12.567 min; 416 Q.225

Method 2: 13.408 min; 430 Q.226

Method 1: 12.686 min; 416 Q.227

Method 2: 13.431 min; 430 Q.228

Method 2: 13.346 min; 362 Q.229

Method 2: 11.570 min; 358 Q.230

Method 1: 12.261 min; 372 Q.231

Method 1: 13.535 min; 394 Q.232

Method 1: 13.295 min; 394 Q.233

Method 2: 11.937 min; 422 Q.234

Method 1: 14.173 min; 398 Q.235

Mp 55-57° C. Q.236

Mp 40-42° C. Q.237

Method 1: 8.524 min; 382 Q.238

Method 1: 19.177 min; 430 Q.239

Method 1: 18.583 min; 416 Q.240

Method 1: 10.070 min; 447 Q.241

Method 1: 12.850 min; 446 Q.242

Method 1: 8.079 min; 427 Q.243

Method 1: 12.200 min; 402 Q.244

Method 1: 9.090 min; 356 Q.245

Method 1: 8.672 min; 382 Q.246

Method 1: 11.718 min; 383 Q.247

Method 1: 13.430 min; 368; Cis Q.248

Method 1: 13.051 min; 348; Cis Q.249

Method 1: 14.416 min; 358; Cis Q.250

Method 1: 13.413 min; 342; Cis Q.251

Method 1: 14.420 min; 346; Cis Q.252

Method 1: 13.397 min; 346; Trans Q.253

Method 2: 13.397 min; 342; Trans Q.254

Method 1: 13.300 min; 356 Q.255

Mp 178-180° C. Q.256

Mp 165-168° C.

Q.257

Method 3: 1.42 min; 370 Q.258

Method 3: 1.55 min; 412 Q.259

Method 3: 1.68 min; 454 Q.260

Method 3: 1.34 min; 412; (S) Q.261

Method 3: 1.34 min; 412; (R) Q.262

Ionic liquid Q.263

Method 3: 1.41 min; 410 Q.264

Method 3: 1.42 min; 428 Q.265

Method 3: 1.40 min; 416 Q.266

Method 3: 1.21 min; 411 Q.267

Method 3: 1.55 min: 452 Q.268

Method 3: 1.52 min; 396; Trans Q.269

Method 3: 1.43 min: 430; Cis Q.270

Mp 111-113° C.; Trans Q.271

Method 1: 13.010 min; 372 Q.272

Method 1: 11.512 min; 386 Q.273

Method 1: 14.147 min; 400 Q.274

Method 1: 14.704 min; 414 Q.275

Method 1: 12.441 min; 388 Q.276

Method 1: 12.949 min; 402 Q.277

Method 1: 12.412 min; 388 Q.278

Method 1: 12.930 min; 402 Q.279

Method 1: 11.765 min; 390 Q.280

Method 1: 13.223 min; 376 Q.281

Method 1: 9.144 min; 366 Q.282

Method 1: 9.411 min; 380 Q.283

Method 1: 13.076 min; 404 Q.284

Method 1: 13.397 min; 404 Q.285

Method 1: 12.345 min; 390 Q.286

Method 1: 12.464 min; 390 Q.287

Method 1: 13.376 min; 418 Q.288

Method 2: 12.056 min; 354 Q.289

Method 1: 11.736 min; 412 Q.290

Mp 81-85° C. Q.291

Method 1: 11.782 min; 408 Q.292

Method 1: 12.318 min; 422 Q.293

Method 1: 12.503 min; 366 Q.294

Method 1: 13.526 min; 438 Q.295

Mp 59-62° C. Q.296

Method 1: 11.641 min; 312 Q.297

Method 1: 11.974 min; 326 Q.298

Mp 57-61° C. Q.299

Method 1: 12.313 min; 394 Q.300

Mp 53-56° C. Q.301

Method 1: 12.908 min; 410 Q.302

Method 1: 12.267 min; 440 Q.303

Method 1: 12.897 min; 454 Q.304

Mp 82-86° C. Q.305

Mp 77-81° C. Q.306

Method 1: 12.789 min; 404 Q.307

Method 1: 13.266 min; 418 Q.308

Method 1: 13.998 min; 396 Q.309

Method 1: 13.524 min; 466 Q.310

Method 1: 13.568 min; 462 Q.311

Method 1: 13.806 min; 462 Q.312

Method 1: 14.266 min; 476 Q.313

Method 1: 14.120 min; 476 Q.314

Method 1: 14.042 min; 480 Q.315

Method 1: 12.395 min; 366 Q.316

Method 1: 7.382 min; 352 Q.317

Mp 78-81° C. Q.318

Method 1: 12.537 min; 430 Q.319

Method 1: 12.594 min; 416 Q.320

Mp 27-30° C. Q.321

Method 1: 12.591 min; 390 Q.322

Mp 67-68° C. Q.323

Mp 83-84° C. Q.324

Method 1: 12.813 min; 390 Q.325

Mp 56-57° C. Q.326

Mp 61-62° C. Q.327

Method 1: 13.121 min; 426 Q.328

Liquid Q.329

Method 1: 14.077 min; 480 Q.330

Method 1: 11.439 min; 392 Q.331

Method 1: 11.711 min; 340 Q.332

Method 1: 9.781 min; 382; Isomer 1 Q.333

Method 1: 9.758 min; 382; Isomer 2 Q.334

Method 6: 0.92 min; 396 Q.335

Method 1: 11.804 min; 408 Q.336

Method 1: 8.965 min; 424 Q.337

Mp 104-108° C. Q.338

Method 1: 10.918 min; 331 Q.339

Method 1: 11.312 min; 344 Q.340

Method 1: 12.292 min; 366 Q.341

Method 1: 11.200 min; 290 Q.342

Method 1: 11.930 min; 304 Q.343

Method 1: 14.959 min; 360 Q.344

Method 1: 13.527 min; 418 Q.345

Method 1: 12.808 min; 404 Q.346

Method 1: 13.160 min; 404 Q.347

Method 1: 11.431 min; 312 Q.348

Method 1: 11.698 min; 326 Q.349

Method 1: 12.595 min; 390 Q.350

Method 1: 11.248 min; 312 Q.351

Mp 110-114° C. Q.352

Method 1: 11.715 min; 326 Q.353

Method 1: 12.754 min; 404 Q.354

Method 1: 11.787 min; 326 Q.355

Method 1: 12.370 min; 340 Q.356

Method 1: 12.096 min; 354 Q.357

Method 1: 12.656 min; 368 Q.358

Method 1: 11.887 min; 326 Q.359

Method 1: 12.700 min; 340 Q.360

Method 1: 12.328 min; 340 Q.361

Method 1: 12.882 min; 354 Q.362

Method 1: 15.320 min; 354 Q.363

Method 1: 12.506 min; 341 Q.364

Method 1: 12.385 min; 390 Q.365

Method 1: 13.743 min; 466 Q.366

Method 1: 10.775 min; 328 Q.367

Method 1: 10.377 min; 314 Q.368

Method 1: 11.191 min; 312 Q.369

Mp 120-121° C. Q.370

Method 1: 11.282 min; 423 Q.371

Method 1: 11.875 min; 272 Q.372

Method 1: 10.334 min; 344 Q.373

Method 1: 10.676 min; 358 Q.374

Method 1: 11.096 min; 372 Q.375

Method 1: 11.418 min; 390 Q.376

Method 1: 11.717 min; 413 Q.377

Method 1: 10.791 min; 358 Q.378

Method 1: 12.258 min; 452 Q.379

Mp 168-170° C. Q.380

Method 1: 12.229 min; 304; Trans Q.381

Method 1: 12.388 min; 305; Cis Q.382

Method 1: 12.988 min; 368 Q.383

Method 6: 0.61 min; 336 Q.384

Method 6: 0.67 min; 332 Q.385

Method 3: 1.34 min; 338 Q.386

Method 3: 1.34 min; 424 Q.387

Method 6: 0.55 min; 286 Q.388

Method 6: 0.73 min; 314 Q.389

Method 6: 0.79 min; 328 Q.390

Method 6: 0.79 min; 328 Q.391

Method 6: 0.83 min; 342 Q.392

Method 6: 0.88 min; 356 Q.393

Method 6: 0.69 min; 312 Q.394

Method 6: 0.75 min; 326 Q.395

Method 6: 0.79 min; 420 Q.396

Method 6: 0.60 min; 442 Q.397

Method 6: 0.93 min; 442 Q.398

Method 6: 0.86 min; 392 Q.399

Method 6: 0.89 min; 390 Q.400

Method 6: 0.83 min; 404 Q.401

Method 6: 0.89 min; 404 Q.402

Method 6: 0.88 min; 406 Q.403

Method 6: 0.99 min; 369 Q.404

Method 6: 0.92 min; 406 Q.405

Method 6: 0.54 min; 334 Q.406

Method 1: 8.584 min; 396 Q.407

Method 1: 12.363 min; 392 Q.408

Method 1: 12.632 min; 319; Trans Q.409

Method 1: 12.533 min; 319; Cis Q.410

Method 1: 11.796 min; 304 Q.411

Method 1: 12.661 min; 318 Q.412

Method 1: 14.132 min; 348 Q.413

Method 1: 14.531 min; 362 Q.414

Method 1: 12.019 min; 304 Q.415

Mp 81-83° C. Q.416

Method 1: 14.621 min; 410 Q.417

Method 1: 15.162 min; 404 Q.418

Method 1: 14.413 min; 340 Q.419

Method 1: 13.860 min; 326 Q.420

Method 1: 13.191 min; 418 Q.421

Method 1: 12.542 min; 354 Q.422

Mp 61-63° C. Q.423

Method 1: 12.785 min; 340 Q.424

Method 1: 12.041 min; 326 Q.425

Method 1: 13.378 min; 418 Q.426

Method 1: 13.958 min; 432 Q.427

Method 1: 8.845 min; 374 Q.428

Method 1: 13.142 min; 370 Q.429

Method 1: 10.416 min; 358 Q.430

Mp 122-124° C. Q.431

Method 1: 10.943 min; 310 Q.432

Method 1: 11.341 min; 324 Q.433

Method 1: 12.746 min; 356 Q.434

Method 1: 10.964 min; 278 Q.435

Method 1: 10.497 min; 264 Q.436

Method 1: 12.277 min; 390 Q.437

Method 1: 12.606 min; 368 Q.438

Method 1: 9.727 min; 370 Q.439

Method 1: 12.860 min; 404 Q.440

Method 1: 10.054 min; 262 Q.441

Method 1: 12.781 min; 276 Q.442

Method 1: 13.922 min; 326 Q.443

Method 1: 12.141 min; 342 Q.444

Method 1: 12.715 min; 356 Q.445

Method 1: 11.909 min; 412 Q.446

Method 1: 9.174 min; 356 Q.447

Method 1: 9.174 min; 356 Q.448

Mp 106-107° C. Q.449

Method 1: 12.070 min; 354 Q.450

Method 1: 12.652 min; 368 Q.451

Method 1: 10.212 min; 358 Q.452

Method 1: 11.435 min; 324 Q.453

Method 1: 11.704 min; 338 Q.454

Mp 85-87° C.

Biological Examples Blumeria qraminis f. sp. tritici (Erysiphe graminis f. sp. tritici)/Wheat/Leaf Disc Preventative (Powdery Mildew on Wheat)

Wheat leaf segments cv. Kanzler were placed on agar in a multiwell plate (24-well format) and sprayed with the formulated test compound diluted in water. The leaf disks were inoculated by shaking powdery mildew infected plants above the test plates 1 day after application. The inoculated leaf disks were incubated at 20° C. and 60% rh under a light regime of 24 h darkness followed by 12 h light/12 h darkness in a climate chamber and the activity of a compound was assessed as percent disease control compared to untreated when an appropriate level of disease damage appears on untreated check leaf segments (6-8 days after application).

The following compounds gave at 200 ppm give at least 50% disease control in this test when compared to untreated control leaf disks under the same conditions, which show extensive disease development:

Q.001, Q.004, Q.005, Q.006, Q.007, Q.010, Q.011, Q.012, Q.013, Q.014, Q.015, Q.016, Q.017, Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024, Q.025, Q.026, Q.027, Q.028, Q.029, Q.030, Q.031, Q.032, Q.033, Q.034, Q.035, Q.036, Q.037, Q.038, Q.039, Q.040, Q.041, Q.042, Q.043, Q.044, Q.045, Q.046, Q.047, Q.048, Q.049, Q.050, Q.051, Q.052, Q.053, Q.054, Q.055, Q.057, Q.058, Q.059, Q.060, Q.062, Q.063, Q.064, Q.065, Q.066, Q.067, Q.068, Q.069, Q.070, Q.071, Q.072, Q.073, Q.074, Q.075, Q.076, Q.077, Q.078, Q.079, Q.080, Q.081, Q.082, Q.084, Q.085, Q.086, Q.087, Q.088, Q.089, Q.090, Q.091, Q.092, Q.093, Q.094, Q.095, Q.097, Q.098, Q.099, Q.100, Q.101, Q.102, Q.103, Q.104, Q.105, Q.106, Q.108, Q.109, Q.110, Q.111, Q.112, Q.113, Q.114, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120, Q.121, Q.122, Q.123, Q.124, Q.125, Q.126, Q.127, Q.128, Q.129, Q.130, Q.131, Q.132, Q.133, Q.134, Q.135, Q.136, Q.140, Q.141, Q.142, Q.143, Q.144, Q.145, Q.146, Q.147, Q.148, Q.149, Q.151, Q.152, Q.153, Q.154, Q.155, Q.156, Q.158, Q.160, Q.161, Q.162, Q.163, Q.164, Q.165, Q.166, Q.167, Q.168, Q.170, Q.171, Q.172, Q.174, Q.175, Q.176, Q.177, Q.178, Q.179, Q.180, Q.181, Q.183, Q.184, Q.185, Q.186, Q.187, Q.188, Q.191, Q.192, Q.193, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201, Q.202, Q.203, Q.204, Q.205, Q.206, Q.207, Q.208, Q.209, Q.211, Q.212, Q.213, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221, Q.222, Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.230, Q.231, Q.233, Q.235, Q.238, Q.239, Q.240, Q.241, Q.242, Q.243, Q.244, Q.245, Q.246, Q.247, Q.248, Q.249, Q.250, Q.251, Q.255, Q.256, Q.260, Q.261, Q.262, Q.263, Q.265, Q.267, Q.269, Q.270, Q.271, Q.272, Q.273, Q.274, Q.275, Q.276, Q.277, Q.278, Q.280, Q.281, Q.282, Q.283, Q.284, Q.285, Q.286, Q.287, Q.288, Q.289, Q.290, Q.291, Q.292, Q.293, Q.294, Q.296, Q.297, Q.298, Q.299, Q.300, Q.301, Q.302, Q.303, Q.304, Q.305, Q.306, Q.307, Q.308, Q.309, Q.310, Q.312, Q.315, Q.316, Q.317, Q.318, Q.319, Q.320, Q.321, Q.322, Q.323, Q.324, Q.325, Q.326, Q.327, Q.329, Q.330, Q.331, Q.332, Q.333, Q.334, Q.335, Q.336, Q.337, Q.338, Q.339, Q.340, Q.341, Q.342, Q.343, Q.344, Q.345, Q.346, Q.347, Q.349, Q.350, Q.351, Q.352, Q.353, Q.354, Q.355, Q.356, Q.357, Q.358, Q.359, Q.360, Q.361, Q.364, Q.365, Q.367, Q.368, Q.369, Q.370, Q.371, Q.373, Q.374, Q.375, Q.376, Q.378, Q.380, Q.381, Q.382, Q.383, Q.384, Q.385, Q.386, Q.388, Q.389, Q.390, Q.391, Q.392, Q.393, Q.394, Q.397, Q.398, Q.400, Q.401

Puccinia recondita f. sp. tritici/Wheat/Leaf Disc Preventative (Brown Rust)

Wheat leaf segments cv. Kanzler were placed on agar in multiwell plates (24-well format) and sprayed with the formulated test compound diluted in water. The leaf disks were inoculated with a spore suspension of the fungus 1 day after application. The inoculated leaf segments were incubated at 19° C. and 75% rh under a light regime of 12 h light/12 h darkness in a climate cabinet and the activity of a compound was assessed as percent disease control compared to untreated when an appropriate level of disease damage appears in untreated check leaf segments (7-9 days after application).

The following compounds gave at 200 ppm gave at least 50% disease control in this test when compared to untreated control leaf disks under the same conditions, which show extensive disease development:

Q.001, Q.002, Q.003, Q.004, Q.005, Q.006, Q.007, Q.008, Q.009, Q.010, Q.011, Q.012, Q.013, Q.014, Q.015, Q.016, Q.017, Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024, Q.025, Q.026, Q.027, Q.028, Q.029, Q.030, Q.031, Q.032, Q.033, Q.034, Q.035, Q.036, Q.037, Q.038, Q.039, Q.040, Q.041, Q.042, Q.043, Q.044, Q.045, Q.046, Q.047, Q.048, Q.049, Q.050, Q.051, Q.052, Q.053, Q.054, Q.055, Q.056, Q.057, Q.058, Q.059, Q.060, Q.061, Q.062, Q.063, Q.064, Q.065, Q.066, Q.067, Q.068, Q.069, Q.070, Q.071, Q.072, Q.073, Q.074, Q.075, Q.076, Q.077, Q.078, Q.079, Q.080, Q.081, Q.082, Q.083, Q.084, Q.085, Q.086, Q.087, Q.088, Q.089, Q.090, Q.091, Q.092, Q.093, Q.094, Q.095, Q.096, Q.097, Q.098, Q.099, Q.100, Q.101, Q.102, Q.103, Q.104, Q.105, Q.106, Q.107, Q.108, Q.109, Q.110, Q.111, Q.112, Q.113, Q.114, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120, Q.121, Q.122, Q.123, Q.124, Q.125, Q.126, Q.127, Q.128, Q.129, Q.130, Q.131, Q.132, Q.133, Q.134, Q.135, Q.136, Q.137, Q.138, Q.140, Q.141, Q.142, Q.143, Q.144, Q.145, Q.146, Q.147, Q.148, Q.149, Q.150, Q.151, Q.152, Q.153, Q.154, Q.155, Q.156, Q.157, Q.158, Q.159, Q.160, Q.161, Q.162, Q.163, Q.164, Q.165, Q.166, Q.167, Q.168, Q.169, Q.170, Q.171, Q.172, Q.173, Q.174, Q.175, Q.176, Q.177, Q.178, Q.179, Q.180, Q.181, Q.182, Q.183, Q.184, Q.185, Q.186, Q.187, Q.188, Q.189, Q.190, Q.191, Q.192, Q.193, Q.194, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201, Q.202, Q.203, Q.204, Q.205, Q.206, Q.207, Q.208, Q.209, Q.210, Q.211, Q.212, Q.213, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221, Q.222, Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.230, Q.231, Q.232, Q.233, Q.234, Q.235, Q.236, Q.237, Q.238, Q.239, Q.240, Q.241, Q.242, Q.243, Q.244, Q.245, Q.246, Q.247, Q.248, Q.249, Q.250, Q.251, Q.252, Q.253, Q.254, Q.255, Q.256, Q.257, Q.258, Q.259, Q.260, Q.261, Q.262, Q.263, Q.264, Q.265, Q.266, Q.267, Q.268, Q.269, Q.270, Q.271, Q.272, Q.273, Q.274, Q.275, Q.276, Q.277, Q.278, Q.279, Q.280, Q.281, Q.282, Q.283, Q.284, Q.285, Q.286, Q.287, Q.288, Q.289, Q.290, Q.291, Q.292, Q.293, Q.294, Q.295, Q.296, Q.297, Q.298, Q.299, Q.300, Q.301, Q.302, Q.303, Q.304, Q.305, Q.306, Q.307, Q.308, Q.309, Q.310, Q.311, Q.312, Q.313, Q.314, Q.315, Q.316, Q.317, Q.318, Q.319, Q.320, Q.321, Q.322, Q.323, Q.324, Q.325, Q.326, Q.327, Q.328, Q.329, Q.330, Q.331, Q.332, Q.333, Q.334, Q.335, Q.336, Q.337, Q.338, Q.339, Q.340, Q.341, Q.342, Q.343, Q.344, Q.345, Q.346, Q.347, Q.348, Q.349, Q.350, Q.351, Q.352, Q.353, Q.354, Q.355, Q.356, Q.357, Q.358, Q.359, Q.360, Q.361, Q.362, Q.363, Q.364, Q.365, Q.366, Q.367, Q.368, Q.369, Q.370, Q.371, Q.372, Q.373, Q.374, Q.375, Q.376, Q.377, Q.378, Q.379, Q.380, Q.381, Q.382, Q.383, Q.384, Q.385, Q.386, Q.387, Q.388, Q.389, Q.390, Q.391, Q.392, Q.393, Q.394, Q.397, Q.398, Q.400, Q.401

Puccinia recondita f. sp. tritici/Wheat/Leaf Disc Curative (Brown Rust)

Wheat leaf segments cv. Kanzler are placed on agar in multiwell plates (24-well format). The leaf segments are inoculated with a spore suspension of the fungus. Plates were stored in darkness at 19° C. and 75% rh. The formulated test compound diluted in water was applied 1 day after inoculation. The leaf segments were incubated at 19° C. and 75% rh under a light regime of 12 h light/12 h darkness in a climate cabinet and the activity of a compound was assessed as percent disease control compared to untreated when an appropriate level of disease damage appears in untreated check leaf segments (6-8 days after application).

The following compounds gave at 200 ppm gaive at least 50% disease control in this test when compared to untreated control leaf disks under the same conditions, which show extensive disease development:

Q.001, Q.004, Q.005, Q.006, Q.007, Q.010, Q.011, Q.012, Q.013, Q.014, Q.015, Q.016, Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024, Q.025, Q.026, Q.027, Q.028, Q.029, Q.030, Q.031, Q.032, Q.033, Q.034, Q.035, Q.036, Q.037, Q.038, Q.039, Q.040, Q.041, Q.042, Q.043, Q.044, Q.045, Q.046, Q.047, Q.048, Q.049, Q.050, Q.051, Q.052, Q.053, Q.054, Q.055, Q.057, Q.058, Q.059, Q.060, Q.062, Q.063, Q.064, Q.065, Q.066, Q.067, Q.068, Q.069, Q.070, Q.071, Q.072, Q.073, Q.074, Q.075, Q.076, Q.077, Q.078, Q.079, Q.080, Q.081, Q.082, Q.084, Q.085, Q.086, Q.087, Q.088, Q.089, Q.090, Q.091, Q.092, Q.093, Q.094, Q.095, Q.096, Q.097, Q.098, Q.099, Q.100, Q.101, Q.102, Q.103, Q.104, Q.105, Q.106, Q.109, Q.110, Q.111, Q.112, Q.113, Q.114, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120, Q.121, Q.122, Q.123, Q.124, Q.126, Q.127, Q.128, Q.129, Q.130, Q.131, Q.132, Q.133, Q.134, Q.135, Q.136, Q.140, Q.141, Q.143, Q.144, Q.145, Q.146, Q.147, Q.148, Q.149, Q.151, Q.152, Q.153, Q.154, Q.155, Q.156, Q.158, Q.159, Q.160, Q.161, Q.162, Q.163, Q.164, Q.165, Q.166, Q.167, Q.168, Q.169, Q.170, Q.171, Q.172, Q.174, Q.175, Q.176, Q.177, Q.178, Q.179, Q.180, Q.181, Q.182, Q.183, Q.184, Q.185, Q.186, Q.188, Q.191, Q.192, Q.193, Q.194, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201, Q.203, Q.204, Q.205, Q.206, Q.207, Q.208, Q.209, Q.211, Q.212, Q.213, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221, Q.222, Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.230, Q.231, Q.232, Q.233, Q.235, Q.236, Q.238, Q.239, Q.240, Q.241, Q.242, Q.243, Q.244, Q.246, Q.247, Q.248, Q.249, Q.250, Q.251, Q.253, Q.254, Q.255, Q.256, Q.257, Q.258, Q.260, Q.261, Q.262, Q.263, Q.265, Q.269, Q.270, Q.271, Q.273, Q.274, Q.275, Q.276, Q.277, Q.278, Q.279, Q.280, Q.281, Q.282, Q.283, Q.284, Q.285, Q.286, Q.287, Q.288, Q.289, Q.290, Q.291, Q.292, Q.293, Q.294, Q.296, Q.297, Q.298, Q.299, Q.300, Q.301, Q.302, Q.303, Q.304, Q.305, Q.306, Q.307, Q.308, Q.309, Q.310, Q.311, Q.315, Q.316, Q.317, Q.318, Q.319, Q.320, Q.321, Q.322, Q.323, Q.324, Q.325, Q.326, Q.327, Q.329, Q.330, Q.331, Q.332, Q.333, Q.334, Q.335, Q.336, Q.337, Q.338, Q.339, Q.340, Q.341, Q.342, Q.344, Q.345, Q.346, Q.347, Q.348, Q.349, Q.350, Q.351, Q.352, Q.353, Q.354, Q.355, Q.356, Q.357, Q.358, Q.359, Q.360, Q.361, Q.362, Q.363, Q.364, Q.365, Q.366, Q.367, Q.368, Q.369, Q.370, Q.371, Q.372, Q.373, Q.374, Q.375, Q.376, Q.377, Q.378, Q.380, Q.381, Q.382, Q.383, Q.384, Q.385, Q.386, Q.388, Q.389, Q.390, Q.391, Q.392, Q.393, Q.394, Q.397, Q.398, Q.400, Q.401

Pyrenophora teres/Barley/Leaf Disc Preventative (Net Blotch)

Barley leaf segments cv. Hasso were placed on agar in a multiwell plate (24-well format) and sprayed with the formulated test compound diluted in water. The leaf segments were inoculated with a spore suspension of the fungus 2 days after application. The inoculated leaf segments were incubated at 20° C. and 65% rh under a light regime of 12 h light/12 h darkness in a climate cabinet and the activity of a compound was assessed as disease control compared to untreated when an appropriate level of disease damage appears in untreated check leaf segments (5-7 days after application).

The following compounds gave at 200 ppm give at least 50% disease control in this test when compared to untreated control leaf disks under the same conditions, which show extensive disease development:

Q.001, Q.004, Q.005, Q.007, Q.011, Q.012, Q.013, Q.014, Q.015, Q.016, Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024, Q.025, Q.026, Q.027, Q.028, Q.029, Q.032, Q.033, Q.034, Q.035, Q.038, Q.039, Q.041, Q.042, Q.043, Q.044, Q.046, Q.047, Q.052, Q.053, Q.054, Q.055, Q.057, Q.059, Q.062, Q.063, Q.066, Q.067, Q.069, Q.070, Q.071, Q.074, Q.075, Q.076, Q.079, Q.082, Q.086, Q.087, Q.088, Q.089, Q.090, Q.091, Q.093, Q.095, Q.097, Q.099, Q.100, Q.101, Q.102, Q.103, Q.105, Q.106, Q.110, Q.111, Q.113, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120, Q.121, Q.122, Q.124, Q.125, Q.127, Q.128, Q.129, Q.131, Q.133, Q.136, Q.141, Q.143, Q.144, Q.146, Q.148, Q.153, Q.154, Q.155, Q.158, Q.160, Q.161, Q.162, Q.163, Q.164, Q.166, Q.167, Q.168, Q.169, Q.170, Q.174, Q.175, Q.176, Q.178, Q.180, Q.183, Q.184, Q.186, Q.191, Q.193, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201, Q.202, Q.203, Q.204, Q.206, Q.207, Q.208, Q.209, Q.211, Q.212, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221, Q.222, Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.231, Q.232, Q.233, Q.235, Q.236, Q.237, Q.238, Q.240, Q.241, Q.242, Q.243, Q.244, Q.245, Q.246, Q.247, Q.248, Q.249, Q.250, Q.251, Q.252, Q.253, Q.255, Q.256, Q.260, Q.261, Q.262, Q.269, Q.275, Q.277, Q.278, Q.280, Q.282, Q.284, Q.285, Q.286, Q.289, Q.291, Q.292, Q.293, Q.298, Q.299, Q.301, Q.302, Q.304, Q.308, Q.311, Q.315, Q.316, Q.320, Q.322, Q.324, Q.326, Q.329, Q.334, Q.335, Q.336, Q.337, Q.340, Q.344, Q.346, Q.349, Q.352, Q.353, Q.354, Q.355, Q.357, Q.358, Q.361, Q.363, Q.364, Q.366, Q.370, Q.371, Q.375, Q.376, Q.377, Q.378, Q.380, Q.382, Q.386, Q.389, Q.390, Q.391, Q.392, Q.393, Q.394, Q.398, Q.400

In the following Tables ‘Activity (%)’ means the assessed experimental activity (% disease control in this test when compared to untreated control leaf disks under the same conditions, which show extensive disease development) and “P” is the expected value calculated (expected) activity according to the COLBY formula (see above). The column headed ‘S?’ indicates whether or not synergy was observed, with ‘y’ meaning that synergy was observed.

In the following tables, compound (V) is N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, compound (VI) is 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide, compound (VII) is [3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.

Monocraphella nivalis (Syn. Microdochium nivale, Fusarium Nivale), Snow Mould, Foot Rot of Cereals

Conidia of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C. and activity was determined visually after 72 hrs

Q.135 Compound (V) rate ppm rate ppm Activity (%) P S? 0.0625 20 0.03125 0 0.015625 0 0.0078125 0 0.0625 50 0.03125 0 0.0625 0.03125 50 20 y 0.03125 0.03125 50 0 y 0.03125 0.0625 70 50 y 0.015625 0.03125 20 0 y 0.015625 0.0625 70 50 y 0.0078125 0.03125 70 0 y Q.135 Flutriafol rate ppm rate ppm Activity (%) P S? 0.0625 70 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 0.25 100 70 y 0.0625 0.125 90 70 y 0.0625 0.0625 90 70 y 0.0625 0.03125 90 70 y

Q.135 Metconazole rate ppm rate ppm Activity (%) P S? 0.0625 70 0.03125 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.0625 0.25 100 70 y 0.0625 0.125 100 70 y 0.0625 0.0625 100 70 y 0.0625 0.03125 100 70 y 0.0625 0.015625 100 70 y 0.03125 0.125 100 0 y 0.03125 0.0625 70 0 y 0.03125 0.03125 50 0 y 0.03125 0.015625 20 0 y Q.135 Trinexapac-ethyl rate ppm rate ppm Activity (%) P S? 0.0625 50 0.03125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.12625 0 0.0625 2.5 100 50 y 0.0625 1.25 90 50 y 0.0625 0.625 70 50 y 0.0625 0.3125 90 50 y 0.0625 0.15625 90 50 y 0.03125 1.25 20 0 y Q.135 Paclobutrazol rate ppm rate ppm Activity (%) P S? 0.0625 70 0.03125 0 0.015625 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.0625 1.25 100 70 y 0.0625 0.625 100 70 y 0.0625 0.3125 100 70 y 0.0625 0.15625 100 70 y 0.03125 1.25 100 0 y 0.03125 0.625 100 0 y 0.03125 0.3125 50 0 y 0.03125 0.15625 20 0 y 0.015625 0.625 20 0 y

Q.135 cis-Jasmone rate ppm rate ppm Activity (%) P S? 0.0625 50 0.03125 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.0625 1.25 100 50 y 0.0625 0.625 90 50 y 0.0625 0.3125 100 50 y 0.0625 0.15625 100 50 y 0.03125 1.25 100 0 y 0.03125 0.625 50 0 y 0.03125 0.3125 20 0 y Q.135 2,4-D rate ppm rate ppm Activity (%) P S? 0.625 50 0.3125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.625 2.5 100 50 y 0.625 1.25 90 50 y 0.625 0.625 90 50 y 0.625 0.3125 90 50 y 0.625 0.15625 100 50 y 0.3125 1.25 20 0 y Q.135 Azoxystrobin rate ppm rate ppm Activity (%) P S? 0.125 70 0.0625 0 0.00625 70 0.003125 20 0.0015625 0 0.125 0.003125 90 70 y 0.0625 0.00625 100 70 y 0.0625 0.0015625 20 0 y Q.135 Pyraclostrobin rate ppm rate ppm Activity (%) P S? 0.125 70 0.0625 0 0.003125 0 0.0015625 0 0.125 0.003125 90 70 y 0.0625 0.003125 20 0 y 0.0625 0.0015625 20 0 y Q.135 Mandipropamid rate ppm rate ppm Activity (%) P S? 0.125 70 0.0625 20 0.03125 0 0.0625 0 0.03125 0 0.125 0.0625 90 70 y 0.125 0.03125 90 70 y 0.0625 0.0625 20 20 y 0.03125 0.0625 50 0 y Q.135 Carbendazim rate ppm rate ppm Activity (%) P S? 0.125 70 0.0625 20 0.0625 0 0.03125 0 0.0015625 0 0.125 0.0625 90 70 y 0.0625 0.03125 50 20 y 0.0625 0.0015625 50 20 y

Q.135 Fenpropimorph rate ppm rate ppm Activity (%) P S? 0.03125 20 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.0078125 0 0.03125 0.125 100 20 y 0.03125 0.0625 90 20 y 0.03125 0.03125 90 20 y 0.03125 0.015625 70 20 y 0.03125 0.0078125 90 20 y Q.135 Bicyclopyrone rate ppm rate ppm Activity (%) P S? 0.0625 20 0.03125 0 0.3125 0 0.15625 0 0.078125 0 0.0625 0.15625 90 20 y 0.03125 0.078125 20 0 y 0.0625 0.3125 70 20 y Q.135 Copper hydroxide rate ppm rate ppm Activity (%) P S? 0.125 70 0.0625 20 5 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.125 0.3125 100 70 y 0.125 0.625 100 70 y 0.125 1.25 100 70 y 0.0625 0.15625 70 20 y 0.0625 0.3125 70 20 y 0.125 2.5 100 70 y 0.125 5 100 70 y Q.135 Manganese oxide rate ppm rate ppm Activity (%) P S? 0.0625 20 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.0625 0.15625 70 20 y 0.0625 0.3125 50 20 y 0.0625 0.625 20 20 0.0625 1.25 70 20 y 0.0625 2.5 90 20 y

Q.135 Abamectin rate ppm rate ppm Activity (%) P S? 0.0625 20 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.0625 0.15625 70 20 y 0.0625 0.3125 50 20 y 0.0625 0.625 20 20 y 0.0625 1.25 50 20 y 0.0625 2.5 100 20 y Q.135 Thiamethoxam rate ppm rate ppm Activity (%) P S? 0.125 70 0.0625 20 5 0 2.5 0 0.625 0 0.3125 0 0.125 0.3125 100 70 y 0.125 0.625 90 70 y 0.0625 0.3125 50 20 y 0.125 0.25 90 70 y 0.125 0.5 100 70 y 0.0625 0.25 70 20 y Q.135 Mesotrione rate ppm rate ppm Activity (%) P S? 0.0625 20 0.03125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.078125 0 0.0625 0.15625 70 20 y 0.0625 0.3125 70 20 y 0.0625 0.625 50 20 y 0.03125 0.078125 20 0 y 0.03125 0.15625 20 0 y 0.03125 0.3125 0 0 y 0.0625 1.25 70 20 y 0.03125 0.625 20 0 y 0.0625 2.5 90 20 y 0.03125 1.25 20 0 y Q.135 Prothioconazole rate ppm rate ppm Activity (%) P S? 0.0625 70 0.03125 0 0.0125 0 0.00625 0 0.003125 0 0.0015625 0 0.0625 0.0015625 100 70 y 0.0625 0.003125 100 70 y 0.0625 0.00625 100 70 y 0.03125 0.0015625 20 0 y 0.03125 0.003125 20 0 y 0.0625 0.0125 100 70 y 0.03125 0.00625 100 0 y 0.03125 0.0125 100 0 y

Q.135 Propiconazole rate ppm rate ppm Activity (%) P S? 0.0625 70 0.03125 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.0625 0.015625 90 70 y 0.0625 0.03125 100 70 y 0.0625 0.0625 100 70 y 0.03125 0.015625 50 0 y 0.03125 0.03125 20 0 y 0.0625 0.125 100 70 y 0.03125 0.0625 50 0 y 0.0625 0.25 100 70 y 0.03125 0.125 70 0 y Q.135 Glufosinate rate ppm rate ppm Activity (%) P S? 0.0625 70 0.03125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.0625 0.3125 90 70 y 0.0625 0.625 70 70 0.0625 1.25 90 70 y 0.03125 0.625 20 0 y 0.0625 2.5 90 70 y 0.03125 1.25 20 0 y Q.113 Flutriafol rate ppm rate ppm Activity (%) P S? 2 70 1 20 0.5 20 0.25 0 2 0 1 0 0.5 0 0.25 0 2 2 100 70 y 2 1 100 70 y 2 0.5 90 70 y 1 2 90 20 y 1 1 70 20 y 1 0.5 70 20 y 1 0.25 50 20 y 0.5 2 50 20 y 0.25 1 20 0 y

Q.113 Metconazole rate ppm rate ppm Activity (%) P S? 1 50 0.5 20 0.25 0 0.125 0 1 20 0.5 0 0.25 0 0.125 0 1 1 100 60 y 1 0.5 100 50 y 1 0.25 100 50 y 0.5 1 100 36 y 0.5 0.5 100 20 y 0.5 0.25 90 20 y 0.5 0.125 50 20 y 0.25 1 100 20 y 0.25 0.5 70 0 y 0.25 0.25 50 0 y 0.25 0.125 20 0 y 0.125 0.5 50 0 y 0.125 0.25 20 0 y 0.125 0.125 20 0 y Q.113 Paclobutrazol rate ppm rate ppm Activity (%) P S? 1 50 0.5 20 0.25 0 0.125 0 10 0 5 0 2.5 0 1.25 0 1 10 100 50 y 1 5 100 50 y 1 2.5 90 50 y 0.5 10 70 20 y 0.5 5 70 20 y 0.5 2.5 50 20 y 0.5 1.25 50 20 y 0.25 10 50 0 y 0.25 5 50 0 y 0.25 2.5 50 0 y 0.25 1.25 20 0 y 0.125 5 20 0 y 0.125 2.5 20 0 y Q.113 Azoxystrobin rate ppm rate ppm Activity (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.00625 50 0.25 0.00625 70 50 y 0.125 0.00625 70 50 y 0.0625 0.00625 50 50 0.03125 0.00625 100 50 y

Q.113 Penflufen rate ppm rate ppm Activity (%) P S? 1 20 0.5 2 0.25 2 0.125 2 1 20 0.5 0 1 1 50 36 y 0.5 1 50 20 y 0.5 0.5 20 0 y 0.25 1 50 20 y 0.25 0.5 20 0 y 0.125 0.5 20 0 y Q.113 Bixafen rate ppm rate ppm Activity (%) P S? 0.25 0 0.125 0 0.0625 0 0.25 20 0.25 0.25 50 20 y 0.125 0.25 50 20 y 0.0625 0.25 50 20 y Q.113 Fenpropimorph rate ppm rate ppm Activity (%) P S? 0.5 20 0.25 0 1 20 0.5 0 0.25 0 0.125 0 0.0625 0 0.5 1 700 36 y 0.5 0.5 100 20 y 0.5 0.25 100 20 y 0.5 0.125 100 20 y 0.25 1 100 20 y 0.25 0.5 90 0 y 0.25 0.25 70 0 y 0.25 0.125 20 0 y 0.25 0.0625 20 0 y Q.113 Cyprodinil rate ppm rate ppm Activity (%) P S? 0.015625 0 0.0078125 0 0.00390625 0 0.003125 20 0.0015625 0 0.015625 0.003125 50 20 y 0.0078125 0.0015625 20 0 y 0.0078125 0.003125 50 20 y 0.00390625 0.0015625 20 0 y Q.113 Abamectin rate ppm rate ppm Activity (%) P S? 2 70 1 20 0.5 0 20 50 10 0 5 0 2 10 100 70 y 1 5 50 20 y 2 20 100 85 y 1 10 50 20 y 1 20 100 60 y 0.5 10 20 0 y 0.5 20 70 50 y Q.113 Mesotrione rate ppm rate ppm Activity (%) P S? 1 20 0.5 0 5 0 2.5 0 1 2.5 50 20 y 1 5 50 20 y 0.5 2.5 20 0 y

Q.113 Prothioconazole rate ppm rate ppm Activity (%) P S? 0.5 0 0.25 0 0.125 0 0.0125 0 0.5 0.0125 90 0 y 0.25 0.0125 50 0 y 0.125 0.0125 20 0 y Q.113 Propiconazole rate ppm rate ppm Activity (%) P S? 2 70 1 20 0.5 0 0.25 0 1 20 0.5 0 0.25 0 0.125 0 2 0.5 100 70 y 2 1 100 76 y 1 0.25 90 20 y 1 0.5 100 20 y 1 1 100 36 y 0.5 0.125 20 0 y 0.5 0.25 50 0 y 0.5 0.5 90 0 y 0.25 0.125 20 0 y 0.25 0.25 20 0 y 0.5 1 100 20 y 0.25 0.5 50 0 y 0.25 1 90 20 y Q.062 Compound (V) rate ppm rate ppm Activity (%) P S? 0.0625 0 0.03125 0 0.015625 0 0.125 70 0.0625 50 0.03125 0 0.0625 0.125 100 70 y 0.03125 0.0625 70 50 y 0.015625 0.03125 20 0 y 0.03125 0.125 90 70 y 0.015625 0.0625 70 50 y Q.062 Compound (VI) rate ppm rate ppm Activity (%) P S? 0.03125 0 0.015625 0 0.125 50 0.0625 0 0.03125 0.125 70 50 y 0.03125 0.0625 20 0 y 0.015625 0.0625 20 0 y Q.062 Chlorothalonil rate ppm rate ppm Activity (%) P S? 0.5 50 0.25 20 0.125 0 0.125 70 0.0625 20 0.03125 0 0.25 0.0625 50 36 y 0.5 0.125 100 85 y 0.125 0.0625 50 20 y 0.125 0.03125 20 0 y

Q.062 Flutriafol rate ppm rate ppm Activity (%) P S? 0.5 50 0.25 20 0.125 0 0.5 0 0.25 0 0.125 0 0.0625 0 0.5 0.5 90 50 y 0.5 0.25 90 50 y 0.5 0.125 90 50 y 0.25 0.5 50 20 y 0.25 0.25 50 20 y 0.25 0.125 50 20 y 0.25 0.0625 50 20 y 0.125 0.5 20 0 y 0.125 0.25 20 0 y 0.125 0.125 20 0 y 0.125 0.0625 20 0 y Q.062 Metconazole rate ppm rate ppm Activity (%) P S? 0.5 50 0.25 20 0.125 0 0.0625 0 1 20 0.5 0 0.25 0 0.125 0 0.0625 0 0.5 1 100 60 y 0.5 0.5 100 50 y 0.5 0.25 70 50 y 0.5 0.125 100 50 y 0.25 1 100 36 y 0.25 0.5 100 20 y 0.25 0.25 90 20 y 0.25 0.125 20 20 y 0.25 0.0625 50 20 y 0.125 0.5 90 0 y 0.125 0.25 50 0 y 0.125 0.125 20 0 y 0.0625 0.25 20 0 y Q.062 Trinexapac-ethyl rate ppm rate ppm Activity (%) P S? 0.5 70 0.25 20 0.125 0 5 0 2.5 0 1.25 0 0.625 0 0.5 5 90 70 y 0.5 2.5 90 70 y 0.5 1.25 90 70 y 0.25 5 50 20 y 0.25 1.25 50 20 y 0.25 0.625 50 20 y 0.125 5 20 0 y 0.125 2.5 20 0 y

Q.062 Paclobutrazol rate ppm rate ppm Activity (%) P S? 0.5 70 0.25 20 0.125 0 10 0 5 0 2.5 0 1.25 0 0.625 0 0.5 10 100 70 y 0.5 5 100 70 y 0.5 2.5 100 70 y 0.5 1.25 100 70 y 0.25 10 100 20 y 0.25 5 100 20 y 0.25 2.5 90 20 y 0.25 1.25 70 20 y 0.25 0.625 70 20 y 0.125 5 70 0 y 0.125 2.5 70 0 y 0.125 1.25 50 0 y 0.125 0.625 20 0 y Q.062 cis-Jasmone rate ppm rate ppm Activity (%) P S? 0.25 20 0.125 0 5 0 2.5 0 1.25 0 0.625 0 0.25 5 50 20 y 0.25 2.5 50 20 y 0.25 1.25 50 20 y 0.25 0.625 50 20 y 0.125 5 50 0 y 0.125 2.5 50 0 y 0.125 1.25 50 0 y Q.062 2,4-D rate ppm (%) Activity (%) P S? 0.5 70 0.25 20 0.125 0 10 0 5 0 2.5 0 1.25 0 0.625 0 0.5 10 90 70 y 0.5 5 90 70 y 0.5 2.5 90 70 y 0.5 1.25 90 70 y 0.25 10 50 20 y 0.25 5 50 20 y 0.25 2.5 50 20 y 0.25 1.25 50 20 y 0.25 0.625 50 20 y 0.125 5 20 0 y 0.125 2.5 20 0 y 0.125 1.25 20 0 y Q.062 Pyraclostrobin rate ppm rate ppm Activity (%) P S? 0.0625 0 0.03125 0 0.015625 0 0.0125 50 0.00625 0 0.0625 0.0125 70 50 y 0.03125 0.0125 70 50 y 0.03125 0.00625 20 0 y 0.015625 0.00625 20 0 y

Q.062 Penflufen Activity rate ppm rate ppm (%) P S? 2 20 1 0 0.5 0 0.25 0 1 20 0.5 0 2 1 50 36 y 1 0.5 20 0 y 0.5 1 50 20 y 0.25 0.5 20 0 y Q.062 Fenpropimorph Activity rate ppm rate ppm (%) P S? 2 20 1 0 2 20 1 0 0.5 0 0.25 0 2 2 100 36 y 2 1 90 20 y 2 0.5 70 20 y 1 2 70 20 y 1 1 50 0 y 1 0.5 20 0 y 1 0.25 20 0 y Q.062 Abamectin Activity rate ppm rate ppm (%) P S? 1 70 0.5 50 20 50 10 0 5 0 1 5 90 70 y 1 10 100 70 y 1 20 100 85 y 0.5 10 70 50 y 0.5 20 100 75 y Q.062 Mesotrione Activity rate ppm rate ppm (%) P S? 1 70 20 0 10 0 5 0 1 5 90 70 y 1 10 90 70 y 1 20 90 70 y Prothio- Q.062 conazole Activity rate ppm rate ppm (%) P S? 0.5 50 0.25 20 0.125 0 0.0625 0 0.0125 0 0.5 0.0125 100 50 y 0.25 0.0125 100 20 y 0.125 0.0125 50 0 y 0.0625 0.0125 20 0 y

Q.062 Propiconazole Activity rate ppm rate ppm (%) P S? 0.5 50 0.25 20 0.125 0 0.0625 0 1 20 0.5 0 0.25 0 0.125 0 0.0625 0 0.5 0.125 70 50 y 0.5 0.25 100 50 y 0.5 0.5 100 50 y 0.25 0.125 50 20 y 0.25 0.25 70 20 y 0.5 1 100 60 y 0.125 0.0625 20 0 y 0.125 0.125 20 0 y 0.25 0.5 100 20 y 0.125 0.25 50 0 y 0.0625 0.125 20 0 y 0.25 1 100 36 y 0.125 0.5 70 0 y 0.0625 0.25 20 0 y Q.062 Glufosinate Activity rate ppm rate ppm (%) P S? 0.125 0 5 0 2.5 0 1.25 0 0.125 1.25 20 0 y 0.125 2.5 20 0 y 0.125 5 20 0 y

Botrytis cinerea (Gray Mould)

Conidia of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C. and the activity was determined visually after 72 hrs.

Fluxa- Q.135 pyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 50 0.03125 20 0.015625 20 0.0078125 0 0.03125 0.0625 70 50 y 0.015625 0.03125 50 20 y 0.0078125 0.015625 50 20 y 0.00390625 0.0078125 20 0 y 0.015625 0.0625 70 50 y 0.0078125 0.03125 50 20 y 0.00390625 0.015625 50 20 y Compound Q.135 (V) Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.125 70 0.0625 70 0.03125 50 0.015625 20 0.015625 0.03125 70 50 y 0.0078125 0.015625 50 20 y 0.03125 0.125 90 70 y 0.015625 0.0625 70 70 0.0078125 0.03125 70 50 y Q.135 Chlorotalonil Activity rate ppm rate ppm (%) P S? 0.5 20 0.25 0 0.125 0 0.0625 0 0.25 20 0.125 0 0.0625 0 0.5 0.25 90 36 y 0.5 0.125 50 20 y 0.25 0.25 90 20 y 0.25 0.125 50 0 y 0.25 0.0625 20 0 y 0.125 0.25 50 20 y 0.125 0.125 50 0 y 0.125 0.0625 20 0 y 0.0625 0.25 50 20 y 0.0625 0.125 20 0 y 0.0625 0.0625 20 0 y

Q.135 Flutriafol Activity rate ppm rate ppm (%) P S? 1 5 0.5 20 0.25 0 0.125 0 1 0 0.5 0 0.25 0 0.125 0 1 1 100 50 y 1 0.5 100 50 y 1 0.25 100 50 y 0.5 1 90 20 y 0.5 0.5 90 20 y 0.5 0.25 90 20 y 0.5 0.125 70 20 y 0.25 1 70 0 y 0.25 0.5 50 0 y 0.25 0.25 50 0 y 0.25 0.125 50 0 y 0.125 0.5 20 0 y Q.135 Metconazole Activity rate ppm rate ppm (%) P S? 0.125 0 0.0625 0 0.03125 0 0.03125 0 0.015625 0 0.125 0.03125 70 0 y 0.0625 0.03125 50 0 y 0.0625 0.015625 20 0 y 0.03125 0.03125 50 0 y Trinexapac- Q.135 ethyl Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 20 0 10 0 5 0 2.5 0 1.25 0 1 20 90 50 y 1 10 90 50 y 1 5 90 50 y 1 2.5 90 50 y 0.5 20 70 20 y 0.5 10 50 20 y 0.5 5 50 20 y 0.5 2.5 50 20 y 0.5 1.25 50 20 y 0.25 10 20 0 y 0.25 5 20 0 y 0.25 1.25 20 0 y Paclobutr- Q.135 azol Activity rate ppm rate ppm (%) P S? 0.5 20 0.25 0 0.125 0 0.0625 0 2.5 0 1.25 0 0.625 0 0.5 2.5 100 20 y 0.5 1.25 100 20 y 0.25 2.5 100 0 y 0.25 1.25 90 0 y 0.25 0.625 70 0 y 0.125 2.5 100 0 y 0.125 1.25 70 0 y 0.125 0.625 50 0 y 0.0625 2.5 100 0 y 0.0625 1.25 50 0 y

cis- Q.135 Jasmone Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 5 0 2.5 0 1.25 0 0.625 0 1 5 90 50 y 1 2.5 90 50 y 0.5 2.5 50 20 y 0.5 1.25 50 20 y 0.25 1.25 20 0 y 0.25 0.625 20 0 y Q.135 2,4-D Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 10 0 5 0 2.5 0 1 10 90 50 y 1 5 100 50 y 1 2.5 90 50 y 0.5 10 50 20 y 0.5 5 50 20 y 0.5 2.5 50 20 y 0.5 1.25 50 20 y Azoxy- Q.135 strobin Activity rate ppm rate ppm (%) P S? 2 50 1 20 0.5 0 0.25 0 0.2 20 0.1 0 0.05 0 0.025 0 2 0.1 90 50 y 2 0.05 70 50 y 1 0.2 70 36 y 1 0.1 50 20 y 1 0.05 50 20 y 1 0.025 50 20 y 0.5 0.2 50 20 y 0.5 0.1 50 0 y 0.5 0.05 20 0 y 0.5 0.025 20 0 y 0.25 0.1 50 0 y 0.25 0.05 20 0 y 0.25 0.025 20 0 y

Pyraclo- Q.135 strobin Activity rate ppm rate ppm (%) P S? 1 20 0.5 0 0.25 0 0.2 20 0.1 0 0.05 0 0.025 0 1 0.2 70 36 y 1 0.1 50 20 y 1 0.05 50 20 y 1 0.025 50 20 y 0.5 0.2 50 20 y 0.5 0.1 50 0 y 0.5 0.05 20 0 y 0.5 0.025 20 0 y 0.25 0.1 20 0 y 0.25 0.05 20 0 y Picoxy- Q.135 strobin Activity rate ppm rate ppm (%) P S? 1 20 0.5 0 0.25 0 0.125 0 2 50 1 50 0.5 50 0.25 50 1 2 90 60 y 1 1 90 60 y 1 0.5 90 60 y 0.5 2 90 50 y 0.5 1 70 50 y 0.5 0.5 70 50 y 0.5 0.25 70 50 y 0.25 1 70 50 y 0.25 0.58 70 50 y 0.25 0.25 70 50 y 0.125 0.5 70 50 y 0.125 0.25 70 50 y Trifloxy- Q.135 strobin Activity rate ppm rate ppm (%) P S? 0.5 20 0.25 0 0.1 50 0.05 50 0.025 20 0.0125 0 0.5 0.025 50 36 y 0.5 0.0125 50 20 y 0.25 0.1 70 50 y 0.25 0.05 50 50 0.25 0.025 50 20 y 0.25 0.0125 20 0 y Q.135 Fludioxonil Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 70 0.03125 0 0.25 0.0625 100 70 y 0.125 0.0625 100 70 y 0.125 0.03125 50 0 y 0.0625 0.0625 100 70 y 0.0625 0.03125 50 0 y 0.03125 0.0625 100 70 y 0.03125 0.03125 50 0 y

Fenpropi- Q.135 morph Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 0.125 0 0.0625 0 0.25 0 0.125 0 0.0625 0 1 0.25 100 50 y 0.5 0.25 100 20 y 0.5 0.125 100 20 y 0.25 0.25 100 0 y 0.25 0.125 100 0 y 0.25 0.0625 90 0 y 0.125 0.25 100 0 y 0.125 0.125 100 0 y 0.125 0.0625 70 0 y 0.0625 0.25 90 0 y 0.0625 0.125 70 0 y 0.0625 0.0625 20 0 y Bicyclo- Q.135 pyrone Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 5 0 2.5 0 1.25 0 1 2.5 70 50 y 1 5 70 50 y 0.5 1.25 50 20 y 0.5 2.5 50 20 y Copper Q.135 hydroxide Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 5 0 2.5 0 1.25 0 1 2.5 70 50 y 1 5 70 50 y 0.5 1.25 50 20 y 0.5 2.5 50 20 y Q.135 Abamectin Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 20 0 10 0 5 0 2.5 0 1.25 0 1 2.5 90 50 y 1 5 90 50 y 1 10 70 50 y 0.5 1.25 50 20 y 0.5 2.5 70 20 y 0.5 5 50 20 y 1 20 70 50 y 0.25 1.25 20 0 y 0.25 2.5 20 0 y 0.5 10 50 20 y 0.25 5 50 0 y 0.5 20 50 20 y 0.25 10 50 0 y

Thia- Q.135 methoxam Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 2.5 0 1.25 0 0.625 0 1 2.5 70 50 y 0.5 1.25 50 20 y 0.25 0.625 20 0 y Q.135 Mesotrione Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 10 0 5 0 2.5 0 1.25 0 0.625 0 1 2.5 70 50 y 1 5 70 50 y 0.5 1.25 50 20 y 0.5 2.5 50 20 y 0.25 0.625 20 0 y 0.25 1.25 20 0 y 0.5 10 50 20 y Prothio- Q.135 conazole Activity rate ppm rate ppm (%) P S? 0.5 20 0.25 0 0.125 0 0.05 50 0.025 0 0.0125 0 0.00625 0 2 0.05 100 85 y 1 0.025 100 20 y 1 0.05 100 60 y 0.5 0.0125 90 20 y 0.5 0.025 100 20 y 0.5 0.05 100 60 y 0.25 0.00625 50 0 y 0.25 0.0125 70 0 y 0.25 0.025 90 0 y 0.125 0.00625 20 0 y 0.125 0.0125 50 0 y 0.125 0.05 100 50 y 0.125 0.025 70 0 y 0.125 0.05 100 50 y

Propi- Q.135 conazole Activity rate ppm rate ppm (%) P S? 2 70 1 50 0.5 20 0.25 0 0.125 0 0.5 50 0.25 0 0.125 0 0.0625 0 2 0.5 100 85 y 1 0.25 100 20 y 1 0.5 100 60 y 0.5 0.125 70 20 y 0.5 0.25 90 20 y 0.5 0.5 100 60 y 0.25 0.0625 50 0 y 0.25 0.125 70 0 y 0.25 0.25 70 0 y 0.125 0.0625 20 0 y 0.125 0.125 20 0 y 0.25 0.5 90 50 y 0.125 0.25 50 0 y 0.125 0.5 70 50 y Q.135 Glufosinate Activity rate ppm rate ppm (%) P S? 1 20 0.5 0 0.25 0 20 0 10 0 5 0 2.5 0 1 2.5 50 20 y 1 5 50 20 y 0.5 2.5 20 0 y 1 20 50 20 y 0.5 10 20 0 y 0.5 20 20 0 y 0.5 10 20 0 y Pro- Q.135 cymidone Activity rate ppm rate ppm (%) P S? 1 20 0.5 0 0.25 0 2.5 50 1.25 0 1 2.5 100 60 y 0.5 1.25 50 0 y 0.25 2.5 90 50 y

Mandi- Q.135 propamid Activity rate ppm rate ppm (%) P S? 2 70 1 20 0.5 0 20 0 10 0 5 0 2 10 90 70 y 2 20 90 70 y 1 5 50 20 y 1 10 50 20 y 0.5 5 20 0 y 1 20 50 20 y 0.5 10 20 0 y 0.5 20 20 0 y Fluxa- Q.113 pyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 50 0.03125 50 0.015625 20 0.0078125 20 0.03125 0.0625 70 50 y 0.015625 0.03125 70 50 y 0.0078125 0.015625 50 20 y 0.00390625 0.0078125 20 20 0.015625 0.0625 70 50 y 0.0078125 0.03125 70 50 y 0.00390625 0.015625 50 20 y Compound Q.113 (VI) Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.0078125 0 0.0625 70 0.03125 70 0.015625 50 0.0078125 20 0.25 0.0625 90 70 y 0.125 0.0625 90 70 y 0.0625 0.0625 90 70 y 0.03125 0.0625 90 70 y 0.015625 0.0625 90 70 y 0.015625 0.015625 70 50 y 0.015625 0.03125 70 70 0.0078125 0.0078125 50 20 y 0.0078125 0.015625 70 50 y Azoxy- Q.113 strobin Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.25 20 0.125 0 0.5 0.125 20 0 y 0.25 0.125 20 0 y 0.125 0.125 20 0 y 0.125 0.25 50 20 y 0.0625 0.125 20 0 y 0.0625 0.25 50 20 y 0.03125 0.125 20 0 y

Pyraclo- Q.113 strobin Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 70 0.25 50 2 2 90 70 y 1 2 90 70 y 1 0.25 70 50 y 0.5 2 90 70 y Chloro- Q.113 talonil Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.25 20 1 0.25 50 20 y 0.5 0.25 70 20 y 0.25 0.25 70 20 y Q.113 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 2 0 1 0 2 2 50 0 y 2 1 20 0 y 1 2 20 0 y Picoxy- Q.113 strobin Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 50 1 50 0.5 50 2 2 70 50 y 2 1 70 50 y 2 0.5 70 50 y 1 2 70 50 y 1 1 70 50 y 0.5 2 70 50 y Trifloxy- Q.113 strobin Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 50 1 50 0.5 50 2 2 70 50 y 2 1 70 50 y 2 0.5 70 50 y 1 2 70 50 y 1 1 70 50 y 0.5 2 70 50 y

Q.113 Fludioxonil Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 70 0.03125 0 0.25 0.03125 70 70 0.125 0.0625 20 0 y 0.125 0.03125 90 70 y 0.0625 0.0625 90 70 y 0.0625 0.03125 20 0 y 0.03125 0.0625 20 0 y Fenpropi- Q.113 morph Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.5 70 0.25 0 0.125 0 2 0.5 100 70 y 1 0.5 100 70 y 1 0.25 100 0 y 0.5 0.5 100 70 y 0.5 0.25 70 0 y 0.5 0.125 20 0 y 0.25 0.5 100 70 y 0.25 0.25 70 0 y 0.125 0.5 90 70 y 0.125 0.25 20 0 y Propi- Q.113 conazole Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.05 70 0.025 0 2 0.05 90 70 y 1 0.025 50 0 y 1 0.05 90 70 y 0.5 0.025 20 0 y 0.5 0.05 90 70 y 0.25 0.025 0 0 0.25 0.05 100 70 y 0.125 0.025 20 0 y 0.125 0.05 90 70 y Prothio- Q.113 conazole Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.5 50 0.25 0 2 0.5 70 50 y 1 0.25 20 0 y 1 0.5 70 50 y 0.5 0.25 20 0 y 0.5 0.5 70 50 y 0.25 0.25 0 0 0.25 0.5 70 50 y 0.125 0.25 20 0 y

Fluxa- Q.062 pyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.125 70 0.0625 50 0.03125 50 0.015625 20 0.03125 0.0625 70 50 y 0.03125 0.125 90 70 y 0.015625 0.0625 70 50 y 0.0078125 0.03125 70 50 y 0.00390625 0.015625 50 20 y 0.0078125 0.015625 50 20 y Pyraclo- Q.062 strobin Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 70 2 2 90 70 y 1 2 90 70 y 0.5 2 90 70 y Chloro- Q.062 talonil Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.25 20 1 0.25 50 20 y 0.5 0.25 50 20 y 0.25 0.25 50 20 y Q.062 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 0 1 0 0.5 0 2 2 50 0 y 2 1 20 0 y 2 0.5 20 0 y 1 2 20 0 y 0.5 2 20 0 y Paclobutr- Q.062 azol Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.125 0 5 70 2.5 0 1.25 0 1 5 100 70 y 1 2.5 70 0 y 0.5 5 100 70 y 0.5 2.5 20 0 y 0.5 1.25 20 0 y 0.25 5 100 70 y 0.125 5 100 70 y 0.125 2.5 100 0 y

Picoxy- Q.062 strobin Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 50 1 50 0.5 50 2 2 70 50 y 2 1 70 50 y 2 0.5 70 50 y 1 2 70 50 y 1 1 70 50 y 1 0.5 70 50 y 0.5 2 70 50 y 0.5 1 70 50 y Q.062 Fludioxonil Activity rate ppm rate ppm (%) P S? 0.25 0 0.1258 0 0.0625 0 0.03125 0 0.0625 50 0.03125 0 0.25 0.03125 90 50 y 0.125 0.0625 20 0 y 0.125 0.03125 90 50 y 0.0625 0.0625 100 50 y 0.0625 0.03125 20 0 y 0.03125 0.0625 20 0 y Fenpropi- Q.062 morph Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.5 70 0.25 0 0.125 0 2 0.5 100 70 y 1 0.5 100 70 y 1 0.25 100 0 y 0.5 0.5 100 70 y 0.5 0.25 70 0 y 0.5 0.125 20 0 y 0.25 0.5 100 70 y 0.25 0.25 70 0 y 0.125 0.5 90 70 y 0.125 0.25 20 0 y Pro- Q.062 cymidone Activity rate ppm rate ppm (%) P S? 0.125 0 0.0625 0 0.03125 0 0.015625 0 1.25 0 0.625 0 0.3125 0 0.125 1.25 70 0 y 0.0625 1.25 100 0 y 0.03125 1.25 90 0 y 0.015625 0.625 70 0 y 0.015625 0.3125 50 0 y

Prothio- .062 conazole Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.05 50 0.025 0 2 0.05 100 50 y 1 0.025 50 0 y 1 0.05 100 50 y 0.5 0.025 50 0 y 0.5 0.05 90 50 y 0.25 0.025 20 0 y 0.25 0.05 90 50 y 0.125 0.025 20 0 y 0.125 0.05 90 50 y Propicon- Q.062 azole Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.5 50 0.25 0 2 0.5 90 50 y 1 0.25 50 0 y 1 0.5 70 50 y 0.5 0.25 20 0 y 0.5 0.5 70 50 y 0.25 0.25 0 0 0.25 0.5 70 50 y 0.125 0.25 20 0 y

Septoria tritici (Leaf Blotch)

Conidia of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C. and the activity was determined visually after 72 hrs.

Fluxa- Q.135 pyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 20 0.03125 0 0.015625 0 0.03125 0.0625 70 20 y 0.015625 0.03125 20 0 y 0.015625 0.0625 90 20 y 0.0078125 0.03125 50 0 y 0.00390625 0.015625 20 0 y Q.135 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 1 0 0.5 0 2 1 90 0 y 2 0.5 50 0 y 1 1 70 0 y 1 0.5 20 0 y 0.5 1 50 0 y 0.5 0.5 20 0 y

Met- Q.135 conazole % rate ppm rate ppm Activity P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 70 0.03125 0 0.25 0.0625 90 70 y 0.125 0.0625 90 70 y 0.125 0.03125 50 0 y 0.0625 0.0625 100 70 y 0.0625 0.03125 20 0 y 0.03125 0.03125 20 0 y Paclo- Q.135 butrazol Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.125 0 5 50 2.5 0 1.25 0 0.625 0 1 2.5 50 0 y 1 5 70 50 y 0.5 5 90 50 y 0.5 2.5 50 0 y 0.5 1.25 20 0 y 0.25 5 70 50 y 0.25 2.5 50 0 y 0.25 1.25 20 0 y 0.25 0.625 20 0 y 0.125 5 70 50 y 0.125 2.5 50 0 y 0.125 1.25 20 0 y 0.125 0.625 20 0 y Mandi- Q.135 propamid % rate ppm rate ppm Activity P S? 2 0 1 0 0.5 0 0.25 0 0.5 70 2 0.5 700 70 y 1 0.5 90 70 y 0.5 0.5 70 70 0.25 0.5 90 70 y Q.135 Penflufen Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.5 70 0.25 20 0.125 0 2 0.5 100 70 y 1 0.5 90 70 y 1 0.25 70 20 y 0.5 0.25 50 20 y 0.5 0.125 20 0 y Fluaz- Q.135 inam Activity rate ppm rate ppm (%) P S? 0.015625 0 0.0078125 0 0.00390625 0 0.03125 20 0.015625 0 0.015625 0.03125 50 20 y 0.0078125 0.03125 50 20 y 0.0078125 0.015625 20 0 y 0.00390625 0.015625 20 0 y

Fluo- Q.135 pyram Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.25 50 1 0.25 90 50 y 0.5 0.25 70 50 y 0.25 0.25 70 50 y Prothio- Q.135 conazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0125 70 0.5 0.0125 90 70 y 0.25 0.0125 90 70 y 0.125 0.0125 90 70 y 0.0625 0.0125 90 70 y 0.03125 0.0125 90 70 y Propi- Q.135 conazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.125 50 0.5 0.125 90 50 y 0.25 0.125 90 50 y 0.125 0.125 90 50 y 0.0625 0.125 90 50 y 0.03125 0.125 90 50 y Fluxa- Q.113 pyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 20 0.03125 0 0.015625 0 0.03125 0.0625 70 20 y 0.015625 0.03125 20 0 y 0.015625 0.0625 90 20 y 0.0078125 0.03125 50 0 y 0.00390625 0.015625 20 0 y Q.113 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 1 0 0.5 0 2 1 70 0 y 2 0.5 20 0 y 1 1 70 0 y 1 0.5 20 0 y 0.5 1 70 0 y 0.5 0.5 20 0 y

Paclo- Q.113 butrazol Activity rate ppm rate ppm (%) P S? 0.5 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 2.5 50 0.625 0 0.3125 20 0.15625 0 0.5 2.5 90 50 y 0.125 2.5 70 0 y 0.0625 0.625 70 50 y 0.03125 0.15625 20 0 y 0.015625 0.3125 70 20 y Picoxy- Q.113 strobin Activity rate ppm rate ppm (%) P S? 0.0078125 0 0.00390625 0 0.03125 90 0.015625 70 0.0078125 50 0.0078125 0.03125 90 70 y 0.0078125 0.015625 90 70 y 0.00390625 0.0078125 70 50 y Q.113 Fluazinam Activity rate ppm rate ppm (%) P S? 0.015625 0 0.0078125 0 0.00390625 0 0.03125 20 0.015625 0 0.015625 0.03125 50 20 y 0.0078125 0.03125 50 20 y 0.0078125 0.015625 20 0 y 0.00390625 0.015625 20 0 y Q.113 Fludioxonil Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.25 70 1 0.25 90 70 y 0.5 0.25 90 70 y 0.25 0.25 90 70 y Prothio- Q.113 conazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0125 70 0.5 0.0125 90 70 y 0.25 0.0125 90 70 y 0.125 0.0125 90 70 y 0.0625 0.0125 90 70 y 0.03125 0.0125 90 70 y Propi- Q.113 conazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.125 50 0.5 0.125 90 50 y 0.25 0.125 70 50 y 0.125 0.125 70 50 y 0.0625 0.125 70 50 y 0.03125 0.125 70 50 y

Iso- Q.062 pyrazam Activity rate ppm rate ppm (%) P S? 0.0078125 0 0.00390625 0 0.03125 20 0.015625 0 0.0078125 0.03125 70 20 y 0.00390625 0.015625 70 0 y Fluxa- Q.062 pyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 20 0.03125 0 0.015625 0 0.03125 0.0625 70 20 y 0.015625 0.03125 20 0 y 0.015625 0.0625 90 20 y 0.0078125 0.03125 70 0 y 0.00390625 0.015625 20 0 y Q.062 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 1 0 0.5 0 2 1 70 0 y 2 0.5 20 0 y 1 1 70 0 y 1 0.5 20 0 y 0.5 1 70 0 y Met- Q.062 conazole Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 50 0.25 0.0625 70 50 y 0.125 0.0625 70 50 y 0.0625 0.0625 70 50 y 0.03125 0.0625 70 50 y Paclo- Q.062 butrazol Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 10 70 5 70 2.5 20 1.25 0 0.625 0 1 2.5 50 20 y 0.5 10 100 70 y 0.5 2.5 70 20 y 0.5 1.25 20 0 y 0.25 10 100 70 y 0.25 5 100 70 y 0.25 2.5 70 20 y 0.25 0.625 90 0 y

Picoxy- Q.062 strobin Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.015625 70 0.0078125 20 0.03125 0.0078125 50 20 y 0.015625 0.0078125 20 20 0.0078125 0.0078125 70 20 y 0.0078125 0.0015625 100 70 y 0.00390625 0.0078125 90 20 y Q.062 Fluazinam Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 70 0.03125 20 0.015625 0 0.03125 0.0625 90 70 y 0.015625 0.0625 90 70 y 0.015625 0.03125 50 20 y 0.0078125 0.03125 50 20 y 0.0078125 0.015625 20 0 y 0.00390625 0.015625 20 0 y Fluo- Q.062 pyram Activity rate ppm rate ppm (%) P S? 0.125 0 0.0625 0 0.03125 0 0.25 50 0.125 0 0.125 0.25 70 50 y 0.0625 0.25 70 50 y 0.0625 0.125 20 0 y 0.03125 0.125 20 0 y Prothio- Q.062 conazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0125 70 0.5 0.0125 90 70 y 0.25 0.0125 90 70 y 0.125 0.0125 90 70 y 0.0625 0.0125 90 70 y 0.03125 0.0125 90 70 y Propi- Q.062 conazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.125 50 0.5 0.125 90 50 y 0.25 0.125 90 50 y 0.125 0.125 90 50 y 0.0625 0.125 70 50 y 0.03125 0.125 70 50 y

Gaeumannomyces araminis (Take-All of Cereals)

Mycelial fragments of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C. and the activity was determined visually after 48 hrs

Compound Q.113 (V) Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.0625 70 0.03125 20 0.015625 0 0.25 0.0625 90 70 y 0.125 0.03125 50 20 y 0.0625 0.015625 20 0 y 0.0625 0.03125 50 20 y 0.03125 0.0625 90 70 y 0.015625 0.03125 50 20 y Compound Q.062 (V) Activity rate ppm rate ppm (%) P S? 0.015625 0 0.0078125 0 0.00390625 0 0.0625 70 0.03125 20 0.015625 0 0.015625 0.03125 50 20 y 0.0078125 0.015625 20 0 y 0.015625 0.0625 100 70 y 0.0078125 0.03125 70 20 y 0.00390625 0.015625 20 0 y

Pythium ultimum (Damping Off):

Mycelial fragments of the fungus, prepared from a fresh liquid culture, were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C. and the activity was determined visually after 48 hrs

Q.135 Mefenoxam Activity rate ppm rate ppm (%) P S? 0.0625 0 0.03125 0 0.015625 0 0.0078125 0 0.03125 50 0.0625 0.03125 70 50 y 0.03125 0.03125 50 50 0.015625 0.03125 70 50 y 0.0078125 0.03125 70 50 y

Mycosphaerella arachidis (y. Cercospora arachidicola), Brown leaf spot of groundnut (peanut): Conidia of the fungus from cryogenic storage were directly mixed into nutrient broth (PDB potato dextrose broth). After placing a (DMSO) solution of the test compounds into a microtiter plate (96-well format) the nutrient broth containing the fungal spores was added. The test plates were incubated at 24° C. and activity was determined visually after 5-6 days.

Q.135 Sedaxan Activity rate ppm rate ppm (%) P S? 0.0625 50 0.03125 50 0.015625 20 0.0078125 0 0.03125 0 0.015625 0 0.00390625 0 0.0625 0.03125 70 50 y 0.0625 0.015625 70 50 y 0.03125 0.031215 50 50 0.015625 0.00390625 50 20 y 0.0078125 0.00390625 20 0 y Q.135 Fluazinam Activity rate ppm rate ppm (%) P S? 0.0625 50 0.03125 50 0.15625 0 0.0078125 0 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 0.015625 70 50 y 0.03125 0.015625 50 50 y 0.015625 0.03125 20 0 y 0.015625 0.015625 20 0 y 0.015625 0.0078125 50 0 y 0.015625 0.00390625 50 0 y 0.0078125 0.03125 20 0 y 0.0078125 0.00390625 20 0 y Q.135 Fludioxonil Activity rate ppm rate ppm (%) P S? 0.03125 50 0.015625 20 0.0625 0 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.03125 0.015625 70 50 y 0.015625 0.0625 50 20 y 0.015625 0.03125 50 20 y 0.015625 0.015625 50 20 y 0.015625 0.0078125 50 20 y 0.015625 0.00390625 50 20 y Fenpropi- Q.135 morph Activity rate ppm rate ppm (%) P S? 0.0625 70 0.03125 70 0.015625 70 0.0078125 20 0.00390625 0 0.03125 70 0.015625 50 0.0078125 20 0.00390625 20 0.0625 0.015625 100 85 y 0.03125 0.015625 100 85 y 0.015625 0.0078125 90 76 y 0.015625 0.00390625 90 76 y 0.0078125 0.03125 100 76 y 0.0078125 0.0078125 50 36 y 0.0078125 0.00390625 50 36 y 0.00390625 0.015625 70 50 y 0.00390625 0.0078125 50 20 y

Q.135 Cyprodinil % rate ppm rate ppm Activity P S? 0.03125 50 0.015625 20 0.00125 0 0.0625 0 0.003125 0 0.0015625 0 0.00078125 0 0.03125 0.00078125 90 50 y 0.03125 0.0015625 70 50 y 0.03125 0.003125 70 50 y 0.03125 0.00625 70 50 y 0.03125 0.0125 70 50 y 0.015625 0.00078125 50 20 y Q.113 Sedaxan Activity rate ppm rate ppm (%) P S? 0.125 20 0.0625 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.125 0.125 50 20 y 0.0625 0.125 20 0 y 0.0625 0.0625 20 0 y 0.0625 0.03125 20 0 y 0.0625 0.015625 20 0 y Q.113 Fluazinam Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.0625 20 0.03125 0 0.03125 0.0625 50 20 y 0.015625 0.0625 50 20 y 0.0078125 0.03125 20 0 y Q.113 Fludioxonil Activity rate ppm rate ppm (%) P S? 0.5 70 0.25 70 0.125 50 0.0625 20 0.03125 0 0.5 70 0.25 0 0.125 0 0.5 0.25 100 70 y 0.25 0.25 90 70 y 0.125 0.5 100 85 y 0.125 0.25 70 50 y 0.0625 0.25 50 20 y 0.03125 0.125 20 0 y Fenpropi- Q.113 morph Activity rate ppm rate ppm (%) P S? 0.125 50 0.0625 50 0.03125 20 0.015625 0 0.0625 70 0.03125 50 0.125 0.0625 100 85 y 0.125 0.03125 100 75 y 0.0625 0.03125 90 75 y 0.03125 0.0625 100 76 y 0.015625 0.03125 70 50 y Q.062 Bixafen Activity rate ppm rate ppm (%) P S? 0.0625 0 0.03125 0 0.015625 0 0.0625 70 0.03125 50 0.0625 0.0625 90 70 y 0.03125 0.0625 90 70 y 0.015625 0.0625 100 70 y 0.015625 0.03125 70 50 y

Q.062 Fludioxonil Activity rate ppm rate ppm (%) P S? 2 70 1 70 0.5 0 0.25 0 0.125 0 0.5 50 0.25 0 0.125 0 2 0.5 100 85 y 1 0.5 100 85 y 0.5 0.5 100 50 y 0.5 0.25 50 0 y 0.5 0.125 20 0 y 0.25 0.5 70 50 y 0.25 0.25 20 0 y 0.125 0.25 20 0 y Q.062 Cyprodinil Activity rate ppm rate ppm (%) P S? 1 70 0.2 0 0.1 0 0.05 0 0.025 0 1 0.025 90 70 y 1 0.1 90 70 y 1 0.2 90 70 y

Septoria tritici (Leaf Blotch):

After placing solutions of the test compounds (containing 0.2% DMSO) into a microtiter plate (96-well format), an equal amount of the nutrient broth (YBG) was added to each of the well. Finally the fungal spore solution was added. The test plates were incubated at 20° C. The inhibition of growth was determined photometrically after 6 days and the activity calculated in relation to untreated control.

Tebu- Q.135 conazole Activity rate ppm rate ppm (%) P S? 1.25 24 0.625 25 0.3125 35 1.25 0 1.25 1.25 59 24 y 0.625 1.25 51 25 y 0.3125 1.25 54 35 y Epoxi- Q.135 conazole (%) rate ppm rate ppm Activity P S? 1.25 22 0.625 32 0.3125 34 0.15625 29 0.3125 78 0.15625 65 1.25 0.3125 95 83 y 0.625 0.3125 98 85 y 0.625 0.15625 94 76 y 0.3125 0.3125 100 86 y 0.15625 0.3125 100 85 y 0.15625 0.15625 98 75 y

Q.113 Cyproconazole Activity rate ppm rate ppm (%) P S? 10 63 1 84 0.5 64 0.25 0 10 1 100 94 y 10 0.5 100 87 y 10 0.25 86 63 y Prothio- Q.113 conazole Activity rate ppm rate ppm (%) P S? 0.15625 42 0.078125 31 0.0390625 28 0.01953125 15 0.0390625 63 0.01953125 69 0.15625 0.0390625 96 78 y 0.078125 0.0390625 100 74 y 0.078125 0.01953125 100 79 y 0.0390625 0.0390625 99 73 y 0.01953125 0.0390625 100 68 y 0.01953125 0.01953125 93 74 y Epoxi- Q.113 conazole Activity rate ppm rate ppm (%) P S? 1.25 42 0.625 39 0.3125 34 0.15625 34 0.078125 33 0.3125 50 1.25 0.3125 97 71 y 0.625 0.3125 100 70 y 0.3125 0.3125 99 67 y 0.15625 0.3125 99 67 y 0.078125 0.3125 98 67 y Cypro- Q.062 conazole Activity rate ppm rate ppm (%) P S? 5 64 2.5 49 1.25 48 2.5 76 1.25 39 5 1.25 96 78 y 2.5 2.5 100 88 y 2.5 1.25 86 69 y 1.25 2.5 98 88 y 1.25 1.25 87 69 y Prothio- Q.062 conazole Activity rate ppm rate ppm (%) P S? 0.3125 33 0.15625 38 0.0078125 31 0.0625 63 0.03125 9 0.3125 0.0625 88 75 y 0.15625 0.0625 98 77 y 0.078125 0.03125 63 73 y Tebu- Q .062 conazole Activity rate ppm rate ppm (%) P S? 5 57 2.5 41 1.25 51 5 73 2.5 47 5 5 100 89 y 5 2.5 96 77 y 2.5 5 100 84 y 2.5 2.5 81 69 y 1.25 5 99 87 y

Q.062 Prochloraz Activity rate ppm rate ppm (%) P S? 0.625 35 0.3125 37 0.03125 80 0.015625 48 0.625 0.03125 98 87 y 0.625 0.015625 79 66 y 0.3125 0.03125 97 87 y Epoxi- Q.062 conazole Activity rate ppm rate ppm (%) P S? 2.5 48 1.25 51 0.625 48 0.3125 42 0.625 71 0.3125 33 2.5 0.625 98 85 y 1.25 0.3125 77 67 y 0.625 0.3125 79 65 y 0.3125 0.3125 71 61 y Difeno- Q.062 conazole Activity rate ppm rate ppm (%) P S? 0.625 40 0.3125 36 0.15625 39 0.078125 29 0.00390625 32 0.15625 48 0.625 0.15625 89 69 y 0.3125 0.15625 81 67 y 0.15625 0.15625 77 68 y 0.078125 0.15625 81 63 y 0.00390625 0.15625 84 64 y Compound Q.062 (S)-(VII) Activity rate ppm rate ppm (%) P S? 0.625 26 0.3125 22 0.125 62 0.0625 44 0.03125 0

Sclerotinia sclerotiorum on Oilseed Rape, Preventive Treatment

The compound activity was tested under 1 day preventive conditions. Oilseed rape plants with 3 unfolded leafs were sprayed with a track sprayer and 200 I/ha spray volume with the test compounds, either solo or in tankmix as shown in the table below.

1 day after application the plants were infested with a solution of Sclerotinia sclerotiorum mycelium. The plants were placed under plastic hoods and high humidity conditions in a climate chamber at 14 h day/10 h night cycle and 15° C. Disease infestation was evaluated visually 11 days after application and average activity calculated in relation to disease severity on untreated check.

Q.135 Boscalid Activity rate ppm rate g a.i./ha (%) P S? 100 15 50 0 25 0 100 25 50 8 100 100 59 36 y 50 50 49 8 y 25 100 76 25 y 100 50 62 21 y 50 50 92 10 y 25 100 83 25 y 100 50 93 32 y Q.113 Boscalid Activity rate ppm rate g a.i./ha (%) P S? 100 39 50 2 25 2 100 25 50 8 100 100 83 54 y 50 50 89 10 y 25 100 83 26 y 100 50 86 44 y Q.062 Boscalid Activity rate ppm rate g a.i./ha (%) P S? 100 26 50 2 25 0 100 25 50 8 100 100 91 44 y 50 50 92 10 y 25 100 83 25 y 100 50 93 32 y

Sphaerotheca fuliginea (Powdery Mildew) on Cucumber, Preventive Treatment

The compound activity was tested under 2 days preventive conditions. Cucumber plants with unfolded cotyledons were sprayed with a roomsprayer and 40 ml/4 plants spray volume with the test compounds, either solo or in tankmix as shown in the table below.

2 days after application the plants were infested with spores of Sphaerotheca fuliginea. The plants were placed in a climate chamber under 70% rel. humidity, 22° C. and 14 h day/10 h night cycle. Disease infestation was evaluated visually 10 days after application and average activity calculated in relation to disease severity on untreated check.

Acibenzolar-s- Q.135 methyl Activity rate ppm rate ppm (%) P S? 2 0 0.6 0 0.2 0 20 4 6 0 2 0 0.6 0 2 20 49 4 y 2 6 16 0 y 0.6 6 15 0 y 0.6 2 4 0 0.2 2 3 0 Acibenzolar-s- Q.113 methyl Activity rate ppm rate ppm (%) P S? 2 0 0.6 0 0.2 0 20 4 6 0 2 0 0.6 0 2 20 18 4 y 2 6 12 0 y 0.6 6 5 0 0.6 2 7 0 0.2 2 9 0 y Acibenzolar-s- Q.062 methyl Activity rate ppm rate ppm (%) P S? 2 7 0.6 0 0.2 0 20 4 6 0 2 0 0.6 0 2 20 11 11 2 6 4 7 0.6 6 9 0 y 0.6 2 5 0 0.2 2 9 0 y

Fusarium Spp. on Wheat, Preventive Treatment

The compound activity was tested under 1 day preventive condition. Flowering wheat plants were sprayed with a track sprayer and 220 I/ha spray volume with the test compounds, either solo or in tankmix as shown in the table below. The compounds were formulated as standard EC100 and diluted into water to the given spray-dosis.

1 day after application the flowering ears were infested with a mix of spores of Fusarium graminearum and Fusarium culmorum. The plants were placed in a climate chamber under 60% rel. humidity, and 14 h day/10 h night cycle with 23/21° C. Disease infestation was evaluated visually 9 days after application and average activity calculated in relation to disease severity on untreated check.

Activity Compound g a.i./ha (%) P S? Prothioconazole (PTZ)  50 55 Q.062 200 17 Q.135 200 28 Q.113 200 23 Q.151 200 3 PTZ + Q.062 200 + 50 83 63 y PTZ + Q.135 200 + 50 86 68 y PTZ + Q.113 200 + 50 85 65 y PTZ + Q.151 200 + 50 88 56 y

Phakopsora pachyrhizi on Soybean, Preventive Treatment

The compound activity was tested under 1 day preventive conditions. Soybean plants with a fully enfolded first trifoliate leaf were sprayed with a track sprayer and 50 I/ha spray volume with the test compounds, either solo or in tankmix as shown in the table below. 1 day after application leaf discs were cutted from the first trifoliate leaf and placed in multiwell plates on water-agar. 5 leaf discs per treatment where infested with spores of a triazole tolerant soybeanrust strain. The multiwell plates where sealed and placed in an incubator 48 h in darkness and 12 h light/dark cycle afterwards. Rust infestation on leaf discs was evaluated visually 11 days after application and average activity calculated in relation to disease severity on untreated check leaf discs.

Rate Activity Compound (g ai/ha) (%) P S? Cyproconazole 2 53 N/A N/A Cyproconazole   0.5 38 N/A N/A Q.062 2 13 N/A N/A Q.062   0.5 0 N/A N/A Q.063 2 0 N/A N/A Q.063   0.5 0 N/A N/A Q.113 2 25 N/A N/A Q.113   0.5 1 N/A N/A Q.135 2 41 N/A N/A Q.135   0.5 13 N/A N/A Q.062 + 2 + 2 99 59 Yes Cyproconazole Q.062 +  2 + 0.5 78 46 Yes Cyproconazole Q.062 + 0.5 + 2  96 53 Yes Cyproconazole Q.063 + 2 + 2 100 53 Yes Cyproconazole Q.063 +  2 + 0.5 98 38 Yes Cyproconazole Q.063 + 0.5 + 2  98 53 Yes Cyproconazole Q.113 + 2 + 2 100 65 Yes Cyproconazole Q.113 +  2 + 0.5 94 54 Yes Cyproconazole Q.113 + 0.5 + 2  96 54 Yes Cyproconazole Q.135 + 2 + 2 95 72 Yes Cyproconazole Q.135 +  2 + 0.5 98 72 Yes Cyproconazole Q.135 + 0.5 + 2  97 46 Yes Cyproconazole

Septoria tritici on Wheat, Preventive Treatment

Four pots per treatment with 4 plants of the wheat variety Riband in each of 6.5 cm pots have been treated 14 days after sowing with the compounds given in the results table. The compounds were formulated as standard EC100 and diluted into water to the given spray-dosis. One day after application of the compounds solo and in mixture, the plants were infested with spores of Septoria tritici. To enable a good infestation, the plants were covered with a plexiglas hood for 48 h after inoculation. The plants grew in a controlled environment for 14 h at 21° C. during day and 10 h at 19° C. during night. 18 days after application the infestation of the 2^(nd) leaf of each of the plants and of the untreated, infested check was evaluated visually. The activity data in the table then derived from a calculation of the infestation of the means of the 4 plants of 4 repetitions of each of the solo or mixture treatments with the mean of the of the 4 plants of 4 repetitions of the untreated infested check.

Activity ga/ha (%) P S? compound (VII) 27  96 N/A N/A 9 20 3 0 Q.062 27  71 N/A N/A 9 8 3 6 Q.135 27  82 N/A N/A 9 33 3 0 Q.113 27  16 N/A N/A 9 0 3 0 Q.151 27  0 N/A N/A 9 0 3 0 compound (VII) +  9 + 27 98 77 Y Q.062 3 + 9 36 8 Y compound (VII) + 27 + 27 99 99 Q.062 9 + 9 93 26 Y compound (VII) + 27 + 9  97 97 Q.062 9 + 3 58 25 Y compound (VII) +  9 + 27 98 47 Y Q.135 3 + 9 47 0 Y compound (VII) + 27 + 27 100 99 Q.135 9 + 9 92 47 Y compound (VII) + 27 + 9  100 98 Q.135 9 + 3 91 20 Y compound (VII) +  9 + 27 97 33 Y Q.113 3 + 9 38 0 Y compound (VII) + 27 + 27 100 97 Q.113 9 + 9 76 20 Y compound (VII) + 27 + 9  99 96 Q.113 9 + 3 70 20 Y compound (VII) +  9 + 27 97 20 Y Q.151 3 + 9 69 0 Y compound (VII) + 27 + 27 99 96 Q.151 9 + 9 96 20 Y compound (VII) + 27 + 9  99 96 Q.151 9 + 3 71 20 Yes Activity Compound g a.i./ha (%) P S? Difenoconazole 27 5 (DFZ) 9 3 3 0 1 0 0.33 0 Q.062 81 61 27 50 9 26 3 8 1 2 Q.135 81 70 27 52 9 43 3 9 1 0 Q.113 81 53 27 61 9 29 3 0 1 1 Q.151 81 43 27 13 9 0 3 4 1 0 DFZ + 27 + 81 97 63 Y Q.062  9 + 27 49 51 27 + 27 85 52 Y 9 + 9 21 28 27 + 9  61 30 Y 9 + 3 0 10 DFZ + 27 + 81 100 71 Y Q.135  9 + 27 92 54 Y 27 + 27 90 55 Y 9 + 9 42 45 27 + 9  68 46 Y 9 + 3 41 12 Y DFZ + 27 + 81 98 56 Y Q.113  9 + 27 94 62 Y 27 + 27 95 63 Y 9 + 9 69 31 Y 27 + 9  91 32 Y 9 + 3 50 3 Y DFZ + 27 + 81 94 46 Y Q.151  9 + 27 68 15 Y 27 + 27 97 17 Y 9 + 9 64 3 Y 27 + 9  85 5 Y 9 + 3 28 7 Y 

What is claimed is:
 1. A compound of formula (I)

wherein R₁ and R₂ are each independently selected from hydrogen and C₁-C₄ alkyl; or R₁ and R₂ together with the nitrogen atom to which they are connected form pyrrolidine or piperidine; R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, formyl, phenyl, C₂-C₄ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl or C₁-C₆ hydroxyalkyl; R₄ is selected from fluorine, chlorine, bromine, C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₃-C₆ cycloalkyl; R₅ is selected from G⁵, G⁶-G⁷ and G¹⁰-G¹¹; G⁵ is C₃-C₇ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy, C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio; G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more groups independently selected from halogen, CN, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy and C₁-C₆ alkylthio; G⁷ is methylene; G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, OH, SH, CHO, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl. G¹¹ is methylene substituted by at least one group independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy; R₆ is hydrogen; R₇ is selected from hydrogen and C₁-C₄ alkyl; or an agronomically acceptable salt, metallic complex, metalloidic complex, isomer, structural isomer, stereo-isomer, diastereoisomer, enantiomer, tautomer, or N-oxide thereof.
 2. A compound of formula (I) according to claim 1 wherein R₁ and R₂ are each C₁-C₄ alkyl; R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄ alkylsulfonyl; R₄ is selected from methyl, ethyl, methoxy, fluorine and chlorine; R₆ is hydrogen; R₇ is hydrogen or C₁-C₄ alkyl.
 3. A compound of formula (I) according to claim 1 wherein R₁ and R₂ are each independently selected from methyl, ethyl and isopropyl; R₃ represents hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, cyclopropyl, ethynyl or C₁-C₄ alkoxy; R₄ is selected from methyl, methoxy, fluorine and chlorine; R₆ is hydrogen; R₇ is hydrogen.
 4. A compound of formula (I) according to claim 1 wherein R₁ is methyl; R₂ is ethyl; R₃ is selected from hydrogen, bromine, iodine, methyl, CHF₂, cyclopropyl, ethynyl and methoxy; R₄ is methyl; R₆ is hydrogen; R₇ is hydrogen.
 5. A compound of formula (I) according to claim 1 wherein R₅ is G⁵; and G⁵ is C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂ and —CH(CH₃)—CH(CH₃)₂.
 6. A compound according to claim 1 wherein R₅ is G⁶-G⁷; G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more halogen, CHF₂, CF₃ and C₁-C₄ alkyl; and G⁷ is methylene.
 7. A compound according to claim 1 wherein R₅ is G¹⁰-G¹¹; G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, methoxy, CHF₂, CF₃ and OCHF₂ and G¹¹ is methylene substituted by at least one group independently selected from methyl, CF₃ and ethyl.
 8. A compound according to claim 1 wherein R₁ is methyl; R₂ is ethyl; R₃ is selected from hydrogen, bromine, iodine, methyl, CHF₂, cyclopropyl, ethynyl and methoxy; R₄ is methyl; R₅ is selected from G⁵, G⁶-G⁷ and G¹⁰-G¹¹; G⁵ is C₆ cycloalkyl, which is substituted by one or more groups independently selected from ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂ and —CH(CH₃)—CH(CH₃)₂; G⁶ is phenyl, which must be substituted by at least one fluorine and is optionally further substituted by one or more halogen, CHF₂, CF₃ and C₁-C₄ alkyl; G⁷ is methylene; G¹⁰ is phenyl, which is optionally substituted by one or more groups independently selected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, methoxy, CHF₂, CF₃ and OCHF₂; G¹¹ is methylene substituted by at least one group independently selected from methyl, CF₃ and ethyl; R₆ is hydrogen; and R₇ is hydrogen; and agronomically acceptable salts/metallic complexes/metalloidic complexes/isomers/structural isomers/stereo-isomers/diastereoisomers/enantiomers/tautomers/N-oxides of those compounds.
 9. A fungicidal composition comprising a compound of formula (I) according to any one of claims 1 to 8, an inert carrier and, optionally, an adjuvant.
 10. A fungicidal composition, comprising a combination of components A) and B), wherein component A) is a compound of formula (I) as defined in any of claims 1 to 8, and agronomically acceptable salts/metallic complexes/metalloidic complexes/isomers/structural isomers/stereo-isomers/diastereoisomers/enantiomers/tautomers/N-oxides of those compounds, and component B) is a strobilurin fungicide, a sterol biosynthesis inhibitor, a triazole fungicide, a pro-triazole fungicide, a DMI fungicide, a SDHI fungicide, or a compound selected from the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione, Tembotrione, Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese, Cyflufenamid, Tebufloquin and Copper.
 11. A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a compound of formula (I) according to any one of claims 1 to 8 or a fungicidal composition according to claim 9 or claim
 10. 12. A method of protecting natural substances of plant origin, which have been taken from their natural life cycle, and/or their processed forms, which comprises applying to said natural substances of plant origin or their processed forms a compound of formula (I) according to any one of claims 1 to 8 or a fungicidal composition according to claim 9 or claim
 10. 